Variant report

Variant	rs555333015
Chromosome Location	chr19:18391890-18391891
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:203)
CpG islands
(count:61)
Chromatin interactive
region (count:72)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HEY1	chr19:18388695-18394026	HepG2	liver:	n/a	chr19:18390515-18390530 chr19:18392424-18392439 chr19:18393317-18393332
2	HMGN3	chr19:18390210-18393435	K562	blood:	n/a	n/a
3	TAF1	chr19:18391813-18393414	H1-neurons	neurons:	n/a	n/a
4	POLR2A	chr19:18382150-18392613	HepG2	liver:	n/a	n/a
5	MTA3	chr19:18391733-18392779	GM12878	blood:	n/a	n/a
6	POLR2A	chr19:18391803-18392676	HepG2	liver:	n/a	n/a
7	PML	chr19:18391789-18393929	GM12878	blood:	n/a	n/a
8	POLR2A	chr19:18388084-18394020	GM12891	blood:	n/a	n/a
9	ZBTB7A	chr19:18391840-18393420	K562	blood:	n/a	n/a
10	POLR2A	chr19:18391839-18393913	K562	blood:	n/a	n/a
11	MAX	chr19:18391759-18393276	H1-hESC	embryonic stem cell:	n/a	chr19:18392864-18392873
12	POLR2A	chr19:18388625-18393808	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr19:18388631-18392724	GM12878	blood:	n/a	n/a
14	ZBTB7A	chr19:18390650-18393443	K562	blood:	n/a	n/a
15	SIN3AK20	chr19:18391857-18392795	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr19:18391833-18392787	U87	brain:	n/a	n/a
17	POLR2A	chr19:18391737-18394004	HCT-116	colon:	n/a	n/a
18	CBX3	chr19:18391836-18394026	K562	blood:	n/a	n/a
19	POLR2A	chr19:18390853-18392790	GM12878	blood:	n/a	n/a
20	POLR2A	chr19:18388705-18392782	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr19:18390259-18393775	GM18526	blood:	n/a	n/a
22	POLR2A	chr19:18391754-18394016	GM12892	blood:	n/a	n/a
23	YY1	chr19:18391768-18393075	GM12891	blood:	n/a	chr19:18392705-18392714 chr19:18392699-18392708 chr19:18392420-18392434
24	POLR2A	chr19:18385002-18394564	K562	blood:	n/a	n/a
25	POLR2A	chr19:18388996-18393928	HCT-116	colon:	n/a	n/a
26	POLR2A	chr19:18391695-18393937	U87	brain:	n/a	n/a
27	RAD21	chr19:18389217-18393748	SK-N-SH	brain:	n/a	chr19:18392832-18392845
28	POLR2A	chr19:18390838-18393817	A549	lung:	n/a	n/a
29	POLR2A	chr19:18382160-18394577	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr19:18391125-18393932	K562	blood:	n/a	n/a
31	CREB1	chr19:18391777-18393197	A549	lung:	n/a	n/a
32	CREB1	chr19:18391151-18393347	K562	blood:	n/a	n/a
33	ETS1	chr19:18391811-18392660	K562	blood:	n/a	n/a
34	SREBP1	chr19:18391848-18394071	GM12878	blood:	n/a	chr19:18392572-18392586 chr19:18392573-18392587
35	TCF12	chr19:18391794-18394072	A549	lung:	n/a	n/a
36	PAX5	chr19:18391862-18393162	GM12878	blood:	n/a	chr19:18392861-18392878 chr19:18392862-18392880
37	POLR2A	chr19:18388726-18394103	HL-60	blood:	n/a	n/a
38	POLR2A	chr19:18388084-18392768	GM12891	blood:	n/a	n/a
39	POLR2A	chr19:18388733-18393961	HL-60	blood:	n/a	n/a
40	POLR2A	chr19:18389346-18393675	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr19:18390219-18393748	GM18951	blood:	n/a	n/a
42	POLR2A	chr19:18382204-18393752	HUVEC	blood vessel:	n/a	n/a
43	BCLAF1	chr19:18391857-18393449	GM12878	blood:	n/a	chr19:18392420-18392433
44	POLR2A	chr19:18384125-18394577	Hela-S3	cervix:	n/a	n/a
45	MAZ	chr19:18391883-18393631	GM12878	blood:	n/a	chr19:18392864-18392873
46	POLR2A	chr19:18390187-18393807	GM12892	blood:	n/a	n/a
47	RCOR1	chr19:18391890-18393375	GM12878	blood:	n/a	n/a
48	POLR2A	chr19:18388801-18393779	HepG2	liver:	n/a	n/a
49	CREB1	chr19:18390123-18394065	HepG2	liver:	n/a	n/a
50	MAX	chr19:18391784-18394058	HepG2	liver:	n/a	chr19:18392864-18392873

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18391883-18391933	ProgFib	skin:	n/a
2	chr19:18391883-18391933	K562	blood:	n/a
3	chr19:18391883-18391933	HRE	kidney:	n/a
4	chr19:18391883-18391933	ECC-1	luminal epithelium:	n/a
5	chr19:18391883-18391933	HMEC	breast:	n/a
6	chr19:18391883-18391933	SK-N-SH	brain:	n/a
7	chr19:18391883-18391933	BE2_C	brain:	n/a
8	chr19:18391883-18391933	HRCEpiC	kidney:	n/a
9	chr19:18391883-18391933	GM06990	blood:	n/a
10	chr19:18391883-18391933	HCF	heart:	n/a
11	chr19:18391883-18391933	GM12878	blood:	n/a
12	chr19:18391883-18391933	Hepatocyte	liver:	n/a
13	chr19:18391883-18391933	HNPCEpiC	eye:	n/a
14	chr19:18391883-18391933	HRPEpiC	eye:	n/a
15	chr19:18391883-18391933	AG10803	skin:	n/a
16	chr19:18391883-18391933	SKMC	muscle:	n/a
17	chr19:18391883-18391933	NB4	blood:	n/a
18	chr19:18391883-18391933	GM19239	blood:	n/a
19	chr19:18391883-18391933	H1-hESC	embryonic stem cell:	embryo
20	chr19:18391883-18391933	IMR90	lung:	fetal
21	chr19:18391883-18391933	MCF10A-Er-Src	breast:	n/a
22	chr19:18391883-18391933	SK-N-MC	brain:	n/a
23	chr19:18391883-18391933	HL-60	blood:	n/a
24	chr19:18391883-18391933	U87	brain:	n/a
25	chr19:18391883-18391933	AoSMC	blood vessel:	n/a
26	chr19:18391883-18391933	CMK	blood:	n/a
27	chr19:18391883-18391933	LNCaP	prostate:	n/a
28	chr19:18391883-18391933	HCT-116	colon:	n/a
29	chr19:18391883-18391933	AG09319	gingival:	n/a
30	chr19:18391883-18391933	GM12891	blood:	n/a
31	chr19:18391883-18391933	AG04449	skin:	fetal
32	chr19:18391883-18391933	RPTEC	kidney:	n/a
33	chr19:18391883-18391933	PFSK-1	brain:	n/a
34	chr19:18391883-18391933	HepG2	liver:	n/a
35	chr19:18391883-18391933	NH-A	brain:	n/a
36	chr19:18391883-18391933	NT2-D1	testis:	n/a
37	chr19:18391883-18391933	HAEpiC	amniotic membrane:	n/a
38	chr19:18391883-18391933	T-47D	breast:	n/a
39	chr19:18391883-18391933	HEEpiC	esophagus:	n/a
40	chr19:18391883-18391933	ovcar-3	ovarian:	n/a
41	chr19:18391883-18391933	NHDF-neo	bronchial:	n/a
42	chr19:18391883-18391933	SAEC	small airway:	n/a
43	chr19:18391883-18391933	HCM	heart:	n/a
44	chr19:18391883-18391933	HUVEC	blood vessel:	n/a
45	chr19:18391883-18391933	GM12892	blood:	n/a
46	chr19:18391883-18391933	HCPEpiC	choroid plexus:	n/a
47	chr19:18391883-18391933	HEK293	kidney:	embryo
48	chr19:18391883-18391933	AG09309	skin:	n/a
49	chr19:18391883-18391933	NHBE	bronchial:	n/a
50	chr19:18391883-18391933	PANC-1	pancreas:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:18311216..18316508-chr19:18389022..18394678,9	MCF-7	breast:
2	chr19:18385043..18394940-chr19:18518893..18533267,53	K562	blood:
3	chr19:18391567..18392492-chr3:156877711..156878415,2	HCT-116	colon:
4	chr19:18388809..18393836-chr19:18524501..18532718,14	MCF-7	breast:
5	chr19:18388423..18395098-chr19:18483334..18487110,13	K562	blood:
6	chr19:18111348..18112154-chr19:18391784..18392610,2	Hela-S3	cervix:
7	chr19:18331499..18333593-chr19:18390857..18393584,2	MCF-7	breast:
8	chr19:18388472..18395098-chr19:18481027..18487774,21	K562	blood:
9	chr19:18391038..18394210-chr19:18525828..18530797,8	MCF-7	breast:
10	chr19:18303093..18307365-chr19:18386584..18393500,10	K562	blood:
11	chr1:173793640..173794179-chr19:18391524..18392416,2	Hela-S3	cervix:
12	chr19:18313659..18316582-chr19:18386529..18393683,9	K562	blood:
13	chr19:18260692..18269532-chr19:18383927..18395911,19	K562	blood:
14	chr12:32552095..32552992-chr19:18391097..18392504,4	Hela-S3	cervix:
15	chr19:18391713..18392557-chr19:18433761..18434274,2	MCF-7	breast:
16	chr19:18387676..18394124-chr19:18495437..18503905,30	K562	blood:
17	chr16:89988316..89991221-chr19:18390772..18393694,2	MCF-7	breast:
18	chr19:18391675..18392417-chr2:196521890..196522480,2	Hela-S3	cervix:
19	chr19:18391400..18392944-chr19:18520489..18523439,2	MCF-7	breast:
20	chr11:71498340..71499087-chr19:18391666..18392636,2	Hela-S3	cervix:
21	chr19:18384108..18395354-chr19:18534355..18544725,18	K562	blood:
22	chr19:18207827..18209431-chr19:18390333..18393371,3	K562	blood:
23	chr19:18382564..18395263-chr19:18409643..18446343,165	MCF-7	breast:
24	chr19:18364058..18367893-chr19:18389808..18392798,4	MCF-7	breast:
25	chr19:18388917..18393354-chr19:18447866..18453758,9	MCF-7	breast:
26	chr19:18313702..18316146-chr19:18389721..18392001,2	MCF-7	breast:
27	chr19:18391645..18392776-chr3:149094513..149095492,3	Hela-S3	cervix:
28	chr19:18276990..18278607-chr19:18389377..18392205,2	K562	blood:
29	chr19:18391746..18392429-chr3:194039980..194040635,2	Hela-S3	cervix:
30	chr19:18391524..18392416-chr7:87848560..87849420,2	Hela-S3	cervix:
31	chr19:18334725..18337698-chr19:18389039..18394023,6	K562	blood:
32	chr19:18390025..18394312-chr19:18496571..18499733,6	MCF-7	breast:
33	chr19:18391743..18392810-chr6:30710116..30710770,3	Hela-S3	cervix:
34	chr19:18391886..18392500-chr4:41215744..41216620,2	HCT-116	colon:
35	chr19:17970685..17972578-chr19:18389953..18392713,2	K562	blood:
36	chr16:745015..745591-chr19:18391631..18392278,2	Hela-S3	cervix:
37	chr19:18332417..18336925-chr19:18388887..18394072,11	K562	blood:
38	chr19:18111363..18113248-chr19:18391327..18393546,2	MCF-7	breast:
39	chr19:18387676..18394344-chr19:18495021..18501696,25	K562	blood:
40	chr19:18391389..18392894-chr19:18547544..18549932,2	MCF-7	breast:
41	chr19:18391626..18394860-chr19:18506004..18508591,3	K562	blood:
42	chr19:18383365..18408325-chr19:18518460..18533256,66	K562	blood:
43	chr19:18391867..18392530-chr9:140171723..140172701,3	Hela-S3	cervix:
44	chr1:176176297..176177165-chr19:18391561..18392505,2	Hela-S3	cervix:
45	chr19:18389237..18391890-chr19:18553028..18555362,2	K562	blood:
46	chr19:18390778..18393256-chr19:55897402..55899140,2	MCF-7	breast:
47	chr19:12903017..12903886-chr19:18391760..18392334,2	Hela-S3	cervix:
48	chr19:18234013..18236269-chr19:18390865..18392530,3	MCF-7	breast:
49	chr19:18301148..18305001-chr19:18389528..18394862,10	MCF-7	breast:
50	chr19:18391769..18392269-chr7:75931715..75932351,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
MIR3188	TF binding region
JUND	TF binding region
JUND	CpG island
MIR3188	CpG island
ENSG00000108107	Chromatin interaction
ENSG00000105647	Chromatin interaction
ENSG00000254858	Chromatin interaction
ENSG00000198625	Chromatin interaction
ENSG00000075142	Chromatin interaction
ENSG00000158234	Chromatin interaction
ENSG00000163660	Chromatin interaction
ENSG00000105640	Chromatin interaction
ENSG00000130511	Chromatin interaction
ENSG00000198113	Chromatin interaction
ENSG00000272273	Chromatin interaction
ENSG00000130513	Chromatin interaction
ENSG00000137312	Chromatin interaction
ENSG00000143207	Chromatin interaction
ENSG00000268173	Chromatin interaction
ENSG00000167491	Chromatin interaction
ENSG00000269145	Chromatin interaction
ENSG00000113739	Chromatin interaction
ENSG00000141232	Chromatin interaction
ENSG00000157637	Chromatin interaction
ENSG00000139132	Chromatin interaction
ENSG00000130520	Chromatin interaction
ENSG00000163697	Chromatin interaction
ENSG00000095066	Chromatin interaction
ENSG00000264175	Chromatin interaction
ENSG00000169908	Chromatin interaction
ENSG00000175489	Chromatin interaction
ENSG00000158483	Chromatin interaction
ENSG00000105650	Chromatin interaction
ENSG00000127585	Chromatin interaction
ENSG00000120334	Chromatin interaction
ENSG00000105655	Chromatin interaction
ENSG00000259006	Chromatin interaction
ENSG00000196950	Chromatin interaction
ENSG00000268650	Chromatin interaction
ENSG00000236021	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000200463	Chromatin interaction
ENSG00000117593	Chromatin interaction
ENSG00000130517	Chromatin interaction
ENSG00000107957	Chromatin interaction
ENSG00000105649	Chromatin interaction
ENSG00000228113	Chromatin interaction
ENSG00000256989	Chromatin interaction
ENSG00000106211	Chromatin interaction
ENSG00000105643	Chromatin interaction
ENSG00000221167	Chromatin interaction
ENSG00000258947	Chromatin interaction
ENSG00000099308	Chromatin interaction
ENSG00000216490	Chromatin interaction
ENSG00000239821	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:55 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
2	esv1837595	chr19:18085428-18393682	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
3	nsv911251	chr19:18224729-18422364	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
4	nsv911253	chr19:18240127-18418044	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
5	nsv916325	chr19:18244780-18534927	Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
6	esv3323899	chr19:18343484-18620429	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	162 gene(s)	inside rSNPs	diseases
7	nsv911268	chr19:18351674-18395537	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	103 gene(s)	inside rSNPs	diseases
8	nsv911269	chr19:18351674-18418044	Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	120 gene(s)	inside rSNPs	diseases
9	nsv911270	chr19:18351674-18422364	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	120 gene(s)	inside rSNPs	diseases
10	nsv911271	chr19:18362940-18453124	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	135 gene(s)	inside rSNPs	diseases
11	nsv828472	chr19:18377725-18404131	Flanking Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	117 gene(s)	inside rSNPs	diseases
12	esv1833305	chr19:18378219-18408222	Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	117 gene(s)	inside rSNPs	diseases
13	nsv911272	chr19:18378219-18439383	Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	135 gene(s)	inside rSNPs	diseases
14	nsv578744	chr19:18380072-18392873	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	100 gene(s)	inside rSNPs	diseases
15	esv1793726	chr19:18381600-18400786	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	104 gene(s)	inside rSNPs	diseases
16	nsv911273	chr19:18386798-18454825	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	134 gene(s)	inside rSNPs	diseases
17	esv18473	chr19:18390503-18393159	Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	96 gene(s)	inside rSNPs	diseases
18	esv1819071	chr19:18390863-18392751	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
19	esv1816229	chr19:18390863-18393112	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	93 gene(s)	inside rSNPs	diseases
20	nsv578745	chr19:18391070-18392473	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	87 gene(s)	inside rSNPs	diseases
21	esv1845750	chr19:18391070-18392618	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	88 gene(s)	inside rSNPs	diseases
22	nsv578746	chr19:18391070-18392618	Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	88 gene(s)	inside rSNPs	diseases
23	nsv578747	chr19:18391070-18392642	Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	88 gene(s)	inside rSNPs	diseases
24	esv1791922	chr19:18391070-18392751	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
25	esv1792720	chr19:18391070-18392751	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
26	esv1794227	chr19:18391070-18392751	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
27	esv1794673	chr19:18391070-18392751	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
28	esv1800376	chr19:18391070-18392751	Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
29	esv1820228	chr19:18391070-18392751	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
30	esv1834297	chr19:18391070-18392751	Transcr. at gene 5' and 3' Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
31	esv1835031	chr19:18391070-18392751	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
32	esv1835429	chr19:18391070-18392751	Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
33	esv1836300	chr19:18391070-18392751	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
34	esv1837134	chr19:18391070-18392751	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
35	esv1837877	chr19:18391070-18392751	Weak transcription Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
36	esv1839910	chr19:18391070-18392751	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
37	nsv578748	chr19:18391070-18392751	Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
38	nsv578749	chr19:18391070-18392873	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
39	esv1801759	chr19:18391070-18393112	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	93 gene(s)	inside rSNPs	diseases
40	nsv578750	chr19:18391070-18393112	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	93 gene(s)	inside rSNPs	diseases
41	esv1801478	chr19:18391070-18395537	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	93 gene(s)	inside rSNPs	diseases
42	nsv578751	chr19:18391074-18392618	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	88 gene(s)	inside rSNPs	diseases
43	nsv578752	chr19:18391074-18392642	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	88 gene(s)	inside rSNPs	diseases
44	nsv578753	chr19:18391074-18392751	Transcr. at gene 5' and 3' Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
45	nsv578754	chr19:18391074-18393112	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	93 gene(s)	inside rSNPs	diseases
46	nsv578755	chr19:18391171-18392642	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	88 gene(s)	inside rSNPs	diseases
47	esv1796641	chr19:18391171-18392751	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
48	esv1799012	chr19:18391171-18392751	Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
49	esv1811606	chr19:18391171-18392751	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
50	esv1841049	chr19:18391171-18392751	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18389000-18392000	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
2	chr19:18389000-18392200	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
3	chr19:18389000-18392200	Transcr. at gene 5' and 3'	Pancreatic Islets	Pancreatic Islet
4	chr19:18389600-18392400	Active TSS	HSMMtube	muscle
5	chr19:18389800-18393200	Active TSS	Aorta	Aorta
6	chr19:18389800-18393200	Active TSS	Small Intestine	intestine
7	chr19:18389800-18393600	Active TSS	Ovary	ovary
8	chr19:18389800-18393800	Active TSS	H9 Cell Line	embryonic stem cell
9	chr19:18390000-18392200	Active TSS	Placenta Amnion	Placenta Amnion
10	chr19:18390000-18392400	Active TSS	Gastric	stomach
11	chr19:18390000-18393000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr19:18390000-18393200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr19:18390000-18393200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr19:18390000-18393400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr19:18390000-18393600	Active TSS	Esophagus	oesophagus
16	chr19:18390000-18393800	Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr19:18390000-18394000	Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr19:18390200-18392000	Active TSS	Right Atrium	heart
19	chr19:18390200-18392200	Active TSS	Fetal Kidney	kidney
20	chr19:18390200-18392200	Active TSS	Fetal Lung	lung
21	chr19:18390200-18392200	Active TSS	Stomach Mucosa	stomach
22	chr19:18390200-18392400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr19:18390200-18392400	Active TSS	NH-A	brain
24	chr19:18390200-18392400	Active TSS	NHLF	lung
25	chr19:18390200-18393000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr19:18390200-18393000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr19:18390200-18393000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr19:18390200-18393000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr19:18390200-18393000	Active TSS	Muscle Satellite Cultured Cells	--
30	chr19:18390200-18393000	Active TSS	Cortex derived primary cultured neurospheres	brain
31	chr19:18390200-18393000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr19:18390200-18393000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr19:18390200-18393000	Active TSS	Brain Substantia Nigra	brain
34	chr19:18390200-18393000	Active TSS	Colonic Mucosa	Colon
35	chr19:18390200-18393000	Active TSS	Thymus	Thymus
36	chr19:18390200-18393000	Active TSS	GM12878-XiMat	blood
37	chr19:18390200-18393000	Active TSS	Hela-S3	cervix
38	chr19:18390200-18393000	Active TSS	HSMM	muscle
39	chr19:18390200-18393000	Active TSS	K562	blood
40	chr19:18390200-18393200	Active TSS	H1 Cell Line	embryonic stem cell
41	chr19:18390200-18393200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr19:18390200-18393200	Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr19:18390200-18393200	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr19:18390200-18393200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr19:18390200-18393200	Active TSS	Primary hematopoietic stem cells	blood
46	chr19:18390200-18393200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr19:18390200-18393200	Active TSS	Brain Angular Gyrus	brain
48	chr19:18390200-18393200	Active TSS	Brain Cingulate Gyrus	brain
49	chr19:18390200-18393200	Active TSS	Brain Hippocampus Middle	brain
50	chr19:18390200-18393200	Active TSS	Duodenum Smooth Muscle	Duodenum

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