Variant report

Variant	rs71309624
Chromosome Location	chr19:18391074-18391075
allele	lengthTooLong
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:220)
CpG islands
(count:0)
Chromatin interactive
region (count:55)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:220 , 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	BACH1	chr19:18390820-18391514	H1-hESC	embryonic stem cell:	n/a	n/a
4	MAX	chr19:18390246-18391577	NB4	blood:	n/a	n/a
5	POLR2A	chr19:18382150-18392613	HepG2	liver:	n/a	n/a
6	YY1	chr19:18390829-18391437	K562	blood:	n/a	n/a
7	HCFC1	chr19:18389403-18391720	Hela-S3	cervix:	n/a	n/a
8	JUND	chr19:18390860-18391517	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr19:18389318-18391619	U87	brain:	n/a	n/a
10	POLR2A	chr19:18388084-18394020	GM12891	blood:	n/a	n/a
11	ZBTB7A	chr19:18390712-18391733	ECC-1	luminal epithelium:	n/a	n/a
12	POLR2A	chr19:18388712-18391582	PFSK-1	brain:	n/a	n/a
13	POLR2A	chr19:18388625-18393808	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr19:18388631-18392724	GM12878	blood:	n/a	n/a
15	ZBTB7A	chr19:18390650-18393443	K562	blood:	n/a	n/a
16	MAZ	chr19:18389512-18391564	HepG2	liver:	n/a	n/a
17	TAF1	chr19:18391067-18391575	GM12878	blood:	n/a	n/a
18	POLR2A	chr19:18390853-18392790	GM12878	blood:	n/a	n/a
19	POLR2A	chr19:18390888-18391621	GM10847	blood:	n/a	n/a
20	SP1	chr19:18391004-18391491	A549	lung:	n/a	n/a
21	BCLAF1	chr19:18390116-18391731	GM12878	blood:	n/a	n/a
22	POLR2A	chr19:18388705-18392782	H1-hESC	embryonic stem cell:	n/a	n/a
23	PAX5	chr19:18390822-18391700	GM12878	blood:	n/a	chr19:18391477-18391496
24	POLR2A	chr19:18388652-18391631	U87	brain:	n/a	n/a
25	POLR2A	chr19:18390259-18393775	GM18526	blood:	n/a	n/a
26	GATA1	chr19:18390157-18391673	PBDE	blood:	n/a	n/a
27	POLR2A	chr19:18385002-18394564	K562	blood:	n/a	n/a
28	POLR2A	chr19:18388996-18393928	HCT-116	colon:	n/a	n/a
29	EGR1	chr19:18389743-18391239	HCT-116	colon:	n/a	chr19:18390485-18390499 chr19:18390484-18390497 chr19:18390487-18390496 chr19:18390516-18390526 chr19:18390483-18390498
30	TCF12	chr19:18390998-18391673	ECC-1	luminal epithelium:	n/a	n/a
31	RAD21	chr19:18389217-18393748	SK-N-SH	brain:	n/a	chr19:18392832-18392845
32	POLR2A	chr19:18390838-18393817	A549	lung:	n/a	n/a
33	ZNF143	chr19:18389690-18391503	GM12878	blood:	n/a	chr19:18389908-18389926
34	POLR2A	chr19:18382160-18394577	MCF10A-Er-Src	breast:	n/a	n/a
35	CHD2	chr19:18391030-18391397	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr19:18391038-18391741	ECC-1	luminal epithelium:	n/a	n/a
37	EP300	chr19:18390388-18391637	GM12878	blood:	n/a	chr19:18390518-18390534
38	SIN3AK20	chr19:18389361-18391722	MCF-7	breast:	n/a	n/a
39	NRF1	chr19:18391061-18391628	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr19:18388726-18394103	HL-60	blood:	n/a	n/a
41	POLR2A	chr19:18388084-18392768	GM12891	blood:	n/a	n/a
42	SIN3A	chr19:18390199-18391654	H1-hESC	embryonic stem cell:	n/a	chr19:18390518-18390529
43	POLR2A	chr19:18388733-18393961	HL-60	blood:	n/a	n/a
44	MXI1	chr19:18390219-18391555	GM12878	blood:	n/a	n/a
45	ATF2	chr19:18390026-18391113	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr19:18389346-18393675	HUVEC	blood vessel:	n/a	n/a
47	TBL1XR1	chr19:18389501-18391643	K562	blood:	n/a	n/a
48	STAT1	chr19:18390235-18391490	GM12878	blood:	n/a	n/a
49	POLR2A	chr19:18390219-18393748	GM18951	blood:	n/a	n/a
50	POLR2A	chr19:18382204-18393752	HUVEC	blood vessel:	n/a	n/a

No data

(count:55 , 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	chr19:18391002..18391717-chr19:18433552..18434414,2	MCF-7	breast:
3	chr19:18385043..18394940-chr19:18518893..18533267,53	K562	blood:
4	chr19:18388809..18393836-chr19:18524501..18532718,14	MCF-7	breast:
5	chr19:18388423..18395098-chr19:18483334..18487110,13	K562	blood:
6	chr19:18389169..18391132-chr19:18534059..18535898,2	K562	blood:
7	chr19:18331499..18333593-chr19:18390857..18393584,2	MCF-7	breast:
8	chr19:18388472..18395098-chr19:18481027..18487774,21	K562	blood:
9	chr19:18102794..18104652-chr19:18390002..18391507,2	K562	blood:
10	chr19:18391038..18394210-chr19:18525828..18530797,8	MCF-7	breast:
11	chr19:18303093..18307365-chr19:18386584..18393500,10	K562	blood:
12	chr19:18313659..18316582-chr19:18386529..18393683,9	K562	blood:
13	chr19:18260692..18269532-chr19:18383927..18395911,19	K562	blood:
14	chr19:18387676..18394124-chr19:18495437..18503905,30	K562	blood:
15	chr19:18262621..18264588-chr19:18388729..18391542,2	MCF-7	breast:
16	chr16:89988316..89991221-chr19:18390772..18393694,2	MCF-7	breast:
17	chr19:18384108..18395354-chr19:18534355..18544725,18	K562	blood:
18	chr19:18389852..18391307-chr19:18434096..18435200,12	MCF-7	breast:
19	chr19:18207827..18209431-chr19:18390333..18393371,3	K562	blood:
20	chr19:18382564..18395263-chr19:18409643..18446343,165	MCF-7	breast:
21	chr19:18364058..18367893-chr19:18389808..18392798,4	MCF-7	breast:
22	chr19:18388917..18393354-chr19:18447866..18453758,9	MCF-7	breast:
23	chr19:18390785..18391350-chrX:134783999..134784500,2	MCF-7	breast:
24	chr19:18313702..18316146-chr19:18389721..18392001,2	MCF-7	breast:
25	chr19:18375824..18378589-chr19:18388804..18391228,3	MCF-7	breast:
26	chr19:18223413..18225267-chr19:18389021..18391701,2	MCF-7	breast:
27	chr19:18276990..18278607-chr19:18389377..18392205,2	K562	blood:
28	chr19:18334725..18337698-chr19:18389039..18394023,6	K562	blood:
29	chr19:18390025..18394312-chr19:18496571..18499733,6	MCF-7	breast:
30	chr19:17970685..17972578-chr19:18389953..18392713,2	K562	blood:
31	chr19:18389073..18391254-chr19:18491178..18493280,2	K562	blood:
32	chr19:18332417..18336925-chr19:18388887..18394072,11	K562	blood:
33	chr19:18387676..18394344-chr19:18495021..18501696,25	K562	blood:
34	chr19:18383365..18408325-chr19:18518460..18533256,66	K562	blood:
35	chr19:18389237..18391890-chr19:18553028..18555362,2	K562	blood:
36	chr19:18390778..18393256-chr19:55897402..55899140,2	MCF-7	breast:
37	chr19:18234013..18236269-chr19:18390865..18392530,3	MCF-7	breast:
38	chr19:18301148..18305001-chr19:18389528..18394862,10	MCF-7	breast:
39	chr19:18390819..18392505-chr19:19495105..19497896,2	K562	blood:
40	chr19:18341889..18345577-chr19:18390952..18393616,3	K562	blood:
41	chr19:18206801..18208746-chr19:18390259..18392773,3	K562	blood:
42	chr19:18303589..18305920-chr19:18390305..18393671,4	K562	blood:
43	chr19:18328659..18330867-chr19:18389570..18391557,2	K562	blood:
44	chr19:18388462..18393408-chr19:18545945..18551144,14	K562	blood:
45	chr19:18388807..18393519-chr19:18545945..18551144,10	K562	blood:
46	chr19:18388723..18391469-chr19:18447700..18450655,3	MCF-7	breast:
47	chr19:18342752..18344966-chr19:18388974..18391959,2	K562	blood:
48	chr19:18116541..18118354-chr19:18390841..18393418,2	MCF-7	breast:
49	chr19:18390598..18392958-chr5:172754478..172756300,2	MCF-7	breast:
50	chr19:18302575..18305285-chr19:18390568..18392250,2	MCF-7	breast:

No data

Variant related genes	Relation type
MIR3188	TF binding region
ENSG00000105650	Chromatin interaction
ENSG00000113739	Chromatin interaction
ENSG00000130517	Chromatin interaction
ENSG00000259006	Chromatin interaction
ENSG00000268173	Chromatin interaction
ENSG00000105649	Chromatin interaction
ENSG00000108107	Chromatin interaction
ENSG00000105640	Chromatin interaction
ENSG00000239821	Chromatin interaction
ENSG00000269145	Chromatin interaction
ENSG00000130511	Chromatin interaction
ENSG00000105647	Chromatin interaction
ENSG00000258947	Chromatin interaction
ENSG00000167491	Chromatin interaction
ENSG00000099308	Chromatin interaction
ENSG00000221167	Chromatin interaction
ENSG00000264175	Chromatin interaction
ENSG00000256989	Chromatin interaction
ENSG00000254858	Chromatin interaction
ENSG00000130513	Chromatin interaction
ENSG00000130520	Chromatin interaction
ENSG00000105655	Chromatin interaction
ENSG00000268650	Chromatin interaction
ENSG00000105643	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:45 , 50 per page) page: 1

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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18388800-18391600	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr19:18388800-18391600	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
3	chr19:18389000-18391600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
4	chr19:18389000-18391600	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
5	chr19:18389000-18391600	Transcr. at gene 5' and 3'	Dnd41	blood
6	chr19:18389000-18392000	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
7	chr19:18389000-18392200	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
8	chr19:18389000-18392200	Transcr. at gene 5' and 3'	Pancreatic Islets	Pancreatic Islet
9	chr19:18389600-18392400	Active TSS	HSMMtube	muscle
10	chr19:18389800-18393200	Active TSS	Aorta	Aorta
11	chr19:18389800-18393200	Active TSS	Small Intestine	intestine
12	chr19:18389800-18393600	Active TSS	Ovary	ovary
13	chr19:18389800-18393800	Active TSS	H9 Cell Line	embryonic stem cell
14	chr19:18390000-18391200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr19:18390000-18391200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr19:18390000-18391400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr19:18390000-18392200	Active TSS	Placenta Amnion	Placenta Amnion
18	chr19:18390000-18392400	Active TSS	Gastric	stomach
19	chr19:18390000-18393000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr19:18390000-18393200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr19:18390000-18393200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr19:18390000-18393400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr19:18390000-18393600	Active TSS	Esophagus	oesophagus
24	chr19:18390000-18393800	Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr19:18390000-18394000	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr19:18390200-18391200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr19:18390200-18391200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr19:18390200-18392000	Active TSS	Right Atrium	heart
29	chr19:18390200-18392200	Active TSS	Fetal Kidney	kidney
30	chr19:18390200-18392200	Active TSS	Fetal Lung	lung
31	chr19:18390200-18392200	Active TSS	Stomach Mucosa	stomach
32	chr19:18390200-18392400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr19:18390200-18392400	Active TSS	NH-A	brain
34	chr19:18390200-18392400	Active TSS	NHLF	lung
35	chr19:18390200-18393000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr19:18390200-18393000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr19:18390200-18393000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
38	chr19:18390200-18393000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr19:18390200-18393000	Active TSS	Muscle Satellite Cultured Cells	--
40	chr19:18390200-18393000	Active TSS	Cortex derived primary cultured neurospheres	brain
41	chr19:18390200-18393000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr19:18390200-18393000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr19:18390200-18393000	Active TSS	Brain Substantia Nigra	brain
44	chr19:18390200-18393000	Active TSS	Colonic Mucosa	Colon
45	chr19:18390200-18393000	Active TSS	Thymus	Thymus
46	chr19:18390200-18393000	Active TSS	GM12878-XiMat	blood
47	chr19:18390200-18393000	Active TSS	Hela-S3	cervix
48	chr19:18390200-18393000	Active TSS	HSMM	muscle
49	chr19:18390200-18393000	Active TSS	K562	blood
50	chr19:18390200-18393200	Active TSS	H1 Cell Line	embryonic stem cell

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