Variant report

Variant	nsv911269
Chromosome Location	chr19:18351674-18418044
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5557)
CpG islands
(count:2628)
Chromatin interactive
region (count:288)
LncRNA
region (count:17)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:5557 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:18404248-18404386	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:18389818-18390682	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:18385374-18386212	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:18383373-18383418	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:18415375-18415575	HepG2	liver:	n/a	n/a
6	ARID3A	chr19:18392371-18393431	HepG2	liver:	n/a	n/a
7	ARID3A	chr19:18412094-18412228	HepG2	liver:	n/a	n/a
8	ARID3A	chr19:18403482-18404364	K562	blood:	n/a	n/a
9	ARID3A	chr19:18390153-18390869	K562	blood:	n/a	n/a
10	ARID3A	chr19:18389512-18389527	K562	blood:	n/a	n/a
11	ARID3A	chr19:18362647-18362831	K562	blood:	n/a	n/a
12	ARID3A	chr19:18415360-18415583	K562	blood:	n/a	n/a
13	ARID3A	chr19:18391176-18391455	K562	blood:	n/a	n/a
14	ARID3A	chr19:18414438-18414539	HepG2	liver:	n/a	n/a
15	ARID3A	chr19:18393121-18393316	K562	blood:	n/a	n/a
16	ARID3A	chr19:18392060-18392633	K562	blood:	n/a	n/a
17	ARID3A	chr19:18402417-18402634	K562	blood:	n/a	n/a
18	ATF1	chr19:18385690-18385962	K562	blood:	n/a	n/a
19	ATF1	chr19:18392118-18392822	K562	blood:	n/a	chr19:18392621-18392635
20	ATF1	chr19:18415329-18415688	K562	blood:	n/a	n/a
21	ATF1	chr19:18402472-18403245	K562	blood:	n/a	n/a
22	ATF2	chr19:18392092-18392709	GM12878	blood:	n/a	chr19:18392621-18392635 chr19:18392512-18392523
23	ATF2	chr19:18362549-18362972	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr19:18392068-18393380	GM12878	blood:	n/a	chr19:18392621-18392635 chr19:18392512-18392523
25	ATF2	chr19:18398551-18398949	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr19:18391203-18391608	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr19:18390189-18390978	GM12878	blood:	n/a	n/a
28	ATF2	chr19:18391185-18391577	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr19:18388966-18389246	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr19:18414924-18416112	GM12878	blood:	n/a	n/a
31	ATF2	chr19:18414170-18414578	GM12878	blood:	n/a	n/a
32	ATF2	chr19:18392820-18393104	GM12878	blood:	n/a	n/a
33	ATF2	chr19:18414087-18414700	GM12878	blood:	n/a	n/a
34	ATF2	chr19:18392192-18392765	H1-hESC	embryonic stem cell:	n/a	chr19:18392621-18392635 chr19:18392512-18392523
35	ATF2	chr19:18402252-18403181	GM12878	blood:	n/a	n/a
36	ATF2	chr19:18392818-18393296	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr19:18402630-18403254	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr19:18362559-18362975	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF2	chr19:18391722-18393301	H1-hESC	embryonic stem cell:	n/a	chr19:18392621-18392635 chr19:18392512-18392523
40	ATF2	chr19:18415854-18416349	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF2	chr19:18390173-18391631	GM12878	blood:	n/a	n/a
42	ATF2	chr19:18390026-18391113	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr19:18415316-18415795	GM12878	blood:	n/a	n/a
44	ATF2	chr19:18401021-18401744	GM12878	blood:	n/a	n/a
45	ATF2	chr19:18398596-18398975	H1-hESC	embryonic stem cell:	n/a	n/a
46	ATF2	chr19:18400932-18401662	GM12878	blood:	n/a	n/a
47	ATF2	chr19:18402331-18402716	GM12878	blood:	n/a	n/a
48	ATF2	chr19:18389710-18390929	H1-hESC	embryonic stem cell:	n/a	n/a
49	ATF3	chr19:18415277-18415640	K562	blood:	n/a	chr19:18415436-18415449 chr19:18415436-18415447
50	ATF3	chr19:18392034-18392791	K562	blood:	n/a	chr19:18392510-18392521 chr19:18392622-18392633 chr19:18392511-18392524 chr19:18392508-18392522 chr19:18392625-18392633 chr19:18392619-18392633 chr19:18392621-18392632 chr19:18392625-18392632

(count:2628 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18391301-18391351	MCF10A-Er-Src	breast:	n/a
2	chr19:18392249-18392299	H1-hESC	embryonic stem cell:	embryo
3	chr19:18385502-18385552	PrEC	prostate:	n/a
4	chr19:18416001-18416051	GM06990	blood:	n/a
5	chr19:18389488-18389538	CMK	blood:	n/a
6	chr19:18391301-18391351	MCF10A-Er-Src	breast:	n/a
7	chr19:18392249-18392299	H1-hESC	embryonic stem cell:	embryo
8	chr19:18385502-18385552	PrEC	prostate:	n/a
9	chr19:18416001-18416051	GM06990	blood:	n/a
10	chr19:18389488-18389538	CMK	blood:	n/a
11	chr19:18402668-18402718	Hela-S3	cervix:	n/a
12	chr19:18415538-18415588	GM19239	blood:	n/a
13	chr19:18392249-18392299	AoSMC	blood vessel:	n/a
14	chr19:18391883-18391933	PrEC	prostate:	n/a
15	chr19:18416001-18416051	NB4	blood:	n/a
16	chr19:18392540-18392590	HNPCEpiC	eye:	n/a
17	chr19:18401021-18401071	Caco-2	colon:	n/a
18	chr19:18390607-18390657	HepG2	liver:	n/a
19	chr19:18392866-18392916	CMK	blood:	n/a
20	chr19:18358989-18359039	T-47D	breast:	n/a
21	chr19:18391832-18391882	HepG2	liver:	n/a
22	chr19:18415538-18415588	SAEC	small airway:	n/a
23	chr19:18391832-18391882	ECC-1	luminal epithelium:	n/a
24	chr19:18383319-18383369	SKMC	muscle:	n/a
25	chr19:18371406-18371456	PrEC	prostate:	n/a
26	chr19:18368368-18368418	SK-N-SH_RA	brain:	n/a
27	chr19:18415646-18415696	HAEpiC	amniotic membrane:	n/a
28	chr19:18392866-18392916	LNCaP	prostate:	n/a
29	chr19:18404194-18404244	HRE	kidney:	n/a
30	chr19:18392889-18392939	H1-hESC	embryonic stem cell:	embryo
31	chr19:18404194-18404244	RPTEC	kidney:	n/a
32	chr19:18392889-18392939	HCM	heart:	n/a
33	chr19:18392994-18393044	ProgFib	skin:	n/a
34	chr19:18404194-18404244	SKMC	muscle:	n/a
35	chr19:18368728-18368778	PANC-1	pancreas:	n/a
36	chr19:18415804-18415854	GM06990	blood:	n/a
37	chr19:18392554-18392604	HNPCEpiC	eye:	n/a
38	chr19:18415538-18415588	PrEC	prostate:	n/a
39	chr19:18390991-18391041	NHBE	bronchial:	n/a
40	chr19:18391301-18391351	MCF-7	breast:	n/a
41	chr19:18392889-18392939	Hepatocyte	liver:	n/a
42	chr19:18390607-18390657	HPAEpiC	pulmonary alveolar:	n/a
43	chr19:18415538-18415588	HAEpiC	amniotic membrane:	n/a
44	chr19:18391832-18391882	GM12891	blood:	n/a
45	chr19:18404194-18404244	K562	blood:	n/a
46	chr19:18401021-18401071	MCF10A-Er-Src	breast:	n/a
47	chr19:18369082-18369132	HPAEpiC	pulmonary alveolar:	n/a
48	chr19:18390991-18391041	AG09309	skin:	n/a
49	chr19:18386421-18386471	HRE	kidney:	n/a
50	chr19:18368728-18368778	SK-N-SH_RA	brain:	n/a

(count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr19:18301148..18305001-chr19:18389528..18394862,10	MCF-7	breast:
2	chr19:18337494..18340607-chr19:18385389..18388339,3	K562	blood:
3	chr19:18342794..18343871-chr19:18362298..18363206,3	K562	blood:
4	chr19:18389024..18389840-chr19:18433961..18434770,2	MCF-7	breast:
5	chr19:18361402..18364353-chr19:18432699..18434486,2	MCF-7	breast:
6	chr19:18389875..18390480-chr19:18438810..18439374,3	MCF-7	breast:
7	chr15:65587972..65588859-chr19:18403872..18404756,2	Hela-S3	cervix:
8	chr19:18391626..18394860-chr19:18506004..18508591,3	K562	blood:
9	chr19:18410193..18413577-chr19:18420795..18423567,3	MCF-7	breast:
10	chr19:18361226..18363795-chr19:18390470..18392704,3	MCF-7	breast:
11	chr19:18357951..18359485-chr19:18364086..18366464,2	K562	blood:
12	chr19:18391867..18392530-chr9:140171723..140172701,3	Hela-S3	cervix:
13	chr19:18388917..18393354-chr19:18447866..18453758,9	MCF-7	breast:
14	chr19:18396145..18399548-chr19:18528063..18530226,4	K562	blood:
15	chr17:79268360..79269165-chr19:18391197..18392005,2	Hela-S3	cervix:
16	chr19:18375824..18378589-chr19:18388804..18391228,3	MCF-7	breast:
17	chr19:18413020..18415467-chr19:18499655..18501302,2	MCF-7	breast:
18	chr19:18219225..18221141-chr19:18367564..18369612,2	K562	blood:
19	chr16:89118958..89119704-chr19:18392729..18393373,2	HCT-116	colon:
20	chr19:18388462..18393408-chr19:18545945..18551144,14	K562	blood:
21	chr19:18397375..18399268-chr19:18401136..18404109,3	MCF-7	breast:
22	chr1:176176297..176177165-chr19:18391561..18392505,2	Hela-S3	cervix:
23	chr19:18385043..18394940-chr19:18518893..18533267,53	K562	blood:
24	chr19:18392892..18393517-chr19:18402516..18403075,2	MCF-7	breast:
25	chr19:18399345..18407720-chr19:18430417..18436364,18	MCF-7	breast:
26	chr19:18392200..18392869-chr19:18403826..18404373,3	MCF-7	breast:
27	chr11:71498340..71499087-chr19:18391666..18392636,2	Hela-S3	cervix:
28	chr19:18340431..18342040-chr19:18361348..18362986,2	K562	blood:
29	chr19:18397375..18399268-chr19:18401136..18404109,3	MCF-7	breast:
30	chr19:18388611..18389307-chrX:21958336..21959275,2	Hela-S3	cervix:
31	chr19:18399894..18406849-chr19:18524216..18528146,7	K562	blood:
32	chr19:18401829..18404172-chr19:18534025..18536659,2	K562	blood:
33	chr19:17970685..17972578-chr19:18389953..18392713,2	K562	blood:
34	chr19:18402536..18404490-chr19:18452623..18454131,2	MCF-7	breast:
35	chr19:18389169..18391132-chr19:18534059..18535898,2	K562	blood:
36	chr1:155197037..155198006-chr19:18392015..18392606,2	Hela-S3	cervix:
37	chr19:18391977..18392505-chr19:45927231..45927877,2	Hela-S3	cervix:
38	chr19:18283000..18284595-chr19:18402682..18404527,2	K562	blood:
39	chr19:18388413..18390013-chr19:18483305..18484834,2	MCF-7	breast:
40	chr19:18364058..18367893-chr19:18389808..18392798,4	MCF-7	breast:
41	chr19:18366386..18369590-chr19:18499675..18502630,3	K562	blood:
42	chr19:18390778..18393256-chr19:55897402..55899140,2	MCF-7	breast:
43	chr16:89988316..89991221-chr19:18390772..18393694,2	MCF-7	breast:
44	chr19:18391917..18392846-chr20:48330164..48330962,2	Hela-S3	cervix:
45	chr19:18312262..18317051-chr19:18400963..18403805,6	K562	blood:
46	chr19:18223413..18225267-chr19:18389021..18391701,2	MCF-7	breast:
47	chr19:18283857..18287210-chr19:18388230..18390509,3	K562	blood:
48	chr19:18391959..18392574-chr9:100395508..100396344,3	Hela-S3	cervix:
49	chr19:18400747..18403330-chr19:18449390..18451589,2	MCF-7	breast:
50	chr12:105629542..105630454-chr19:18392234..18393176,2	Hela-S3	cervix:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA1683-1	chr19:18361122-18361282	NONHSAT062947
2	lnc-PGPEP1-5	chr19:18392659-18393560	NONHSAT062954
3	lnc-JUND-1	chr19:18378189-18378375	NONHSAT062952
4	lnc-JUND-1	chr19:18385213-18385240	NONHSAT062952
5	lnc-KIAA1683-1	chr19:18360957-18361282	NONHSAT062948
6	lnc-JUND-1	chr19:18380276-18380397	NONHSAT062952
7	lnc-JUND-1	chr19:18380276-18380397	NONHSAT062951
8	lnc-JUND-1	chr19:18378582-18378777	NONHSAT062952
9	lnc-PGPEP1-3	chr19:18408032-18408552	NONHSAT062958
10	lnc-KIAA1683-1	chr19:18362874-18362971	NONHSAT062947
11	lnc-JUND-1	chr19:18378582-18378777	NONHSAT062951
12	lnc-JUND-1	chr19:18385213-18385240	NONHSAT062951
13	lnc-PGPEP1-4	chr19:18407534-18407915	NONHSAT062957
14	lnc-KIAA1683-1	chr19:18366030-18366229	NONHSAT062947
15	lnc-KIAA1683-1	chr19:18362874-18363242	NONHSAT062948
16	lnc-KIAA1683-1	chr19:18360760-18360987	NONHSAT062947
17	lnc-JUND-1	chr19:18378146-18378336	NONHSAT062951

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3188	chr19:18392939-18392961	MIMAT0015070

No data

Variant related genes	Relation type
KIAA1683	TF binding region
JUND	TF binding region
MIR3188	TF binding region
RPL39P38	TF binding region
PDE4C	TF binding region
KIAA1683	CpG island
JUND	CpG island
MIR3188	CpG island
RPL39P38	CpG island
PDE4C	CpG island
ENSG00000130518	chromatin interactions
ENSG00000111885	chromatin interactions
ENSG00000136925	chromatin interactions
ENSG00000137522	chromatin interactions
ENSG00000012061	chromatin interactions
ENSG00000146085	chromatin interactions
ENSG00000105655	chromatin interactions
ENSG00000113739	chromatin interactions
ENSG00000151881	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000142168	chromatin interactions
ENSG00000105649	chromatin interactions
ENSG00000144043	chromatin interactions
ENSG00000070404	chromatin interactions
ENSG00000177692	chromatin interactions
ENSG00000127585	chromatin interactions
ENSG00000239821	chromatin interactions
ENSG00000236021	chromatin interactions
ENSG00000143702	chromatin interactions
ENSG00000108107	chromatin interactions
ENSG00000106348	chromatin interactions
ENSG00000254469	chromatin interactions
ENSG00000136044	chromatin interactions
ENSG00000130517	chromatin interactions
ENSG00000168807	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000176986	chromatin interactions
ENSG00000158234	chromatin interactions
ENSG00000196576	chromatin interactions
ENSG00000234509	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000086712	chromatin interactions
ENSG00000105642	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000107957	chromatin interactions
ENSG00000228113	chromatin interactions
ENSG00000256982	chromatin interactions
ENSG00000260285	chromatin interactions
ENSG00000182718	chromatin interactions
ENSG00000105647	chromatin interactions
ENSG00000207005	chromatin interactions
ENSG00000168906	chromatin interactions
ENSG00000105650	chromatin interactions
ENSG00000259006	chromatin interactions
ENSG00000269145	chromatin interactions
ENSG00000105656	chromatin interactions
ENSG00000099308	chromatin interactions
ENSG00000256989	chromatin interactions
ENSG00000243678	chromatin interactions
ENSG00000116679	chromatin interactions
ENSG00000100201	chromatin interactions
ENSG00000175489	chromatin interactions
ENSG00000198113	chromatin interactions
ENSG00000105640	chromatin interactions
ENSG00000165476	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000112658	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000105700	chromatin interactions
ENSG00000071462	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000157637	chromatin interactions
ENSG00000163660	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000136937	chromatin interactions
ENSG00000130513	chromatin interactions
ENSG00000254858	chromatin interactions
ENSG00000167491	chromatin interactions
ENSG00000105643	chromatin interactions
ENSG00000106211	chromatin interactions
ENSG00000258947	chromatin interactions
ENSG00000216490	chromatin interactions
ENSG00000143207	chromatin interactions
ENSG00000228384	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000258881	chromatin interactions
ENSG00000196950	chromatin interactions
ENSG00000213523	chromatin interactions
ENSG00000006015	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000130363	chromatin interactions
ENSG00000120334	chromatin interactions
ENSG00000110721	chromatin interactions
ENSG00000198625	chromatin interactions
ENSG00000163697	chromatin interactions
ENSG00000139132	chromatin interactions
ENSG00000031691	chromatin interactions
ENSG00000141232	chromatin interactions
ENSG00000158470	chromatin interactions
ENSG00000268650	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000095066	chromatin interactions
ENSG00000130520	chromatin interactions
ENSG00000169908	chromatin interactions
ENSG00000176410	chromatin interactions
ENSG00000117593	chromatin interactions
ENSG00000073756	chromatin interactions
ENSG00000141526	chromatin interactions
ENSG00000267959	chromatin interactions
ENSG00000037474	chromatin interactions
ENSG00000119403	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000198890	chromatin interactions
ENSG00000075142	chromatin interactions
ENSG00000271913	chromatin interactions
ENSG00000273129	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000268173	chromatin interactions
ENSG00000167196	chromatin interactions
ENSG00000163536	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000264175	chromatin interactions
ENSG00000221167	chromatin interactions
ENSG00000102172	chromatin interactions
ENSG00000130511	chromatin interactions
ENSG00000206737	chromatin interactions
RPLP1	Mature miRNA region

Extended variants
information (count: 3129 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3129 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs172043	chr19:18351674-18351675	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555506573	chr19:18351707-18351708	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs537184339	chr19:18351714-18351715	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs148556739	chr19:18351725-18351726	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs544412929	chr19:18351756-18351757	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs564161307	chr19:18351797-18351798	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs533233671	chr19:18351812-18351813	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs115943735	chr19:18351829-18351830	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs370687928	chr19:18351830-18351831	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs528469936	chr19:18351839-18351840	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs548223282	chr19:18351879-18351880	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs568205624	chr19:18351936-18351937	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs549556652	chr19:18351966-18351967	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs377688355	chr19:18351976-18351977	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs530945900	chr19:18351980-18351981	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs550738685	chr19:18351995-18351996	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs376113665	chr19:18352037-18352038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188218058	chr19:18352045-18352046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536099609	chr19:18352051-18352052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368979506	chr19:18352057-18352058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200717537	chr19:18352066-18352067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550357216	chr19:18352086-18352087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540090465	chr19:18352116-18352117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553398113	chr19:18352139-18352140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566418514	chr19:18352140-18352141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535442164	chr19:18352146-18352147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142906617	chr19:18352158-18352159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575398097	chr19:18352187-18352188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537968031	chr19:18352188-18352189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557907474	chr19:18352205-18352206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs151122934	chr19:18352210-18352211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540473333	chr19:18352213-18352214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544967173	chr19:18352243-18352244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560183573	chr19:18352248-18352249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573638428	chr19:18352268-18352269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375968160	chr19:18352279-18352280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541805919	chr19:18352287-18352288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs56409741	chr19:18352291-18352292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140158511	chr19:18352299-18352300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550809958	chr19:18352311-18352312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564659160	chr19:18352312-18352313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533367724	chr19:18352322-18352323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374994814	chr19:18352329-18352330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547221040	chr19:18352357-18352358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567165326	chr19:18352366-18352367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536191253	chr19:18352369-18352370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182002918	chr19:18352372-18352373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs143601102	chr19:18352373-18352374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117198561	chr19:18352508-18352509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557578146	chr19:18352519-18352520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:3584 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18345000-18358400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:18348600-18385200	Weak transcription	Right Atrium	heart
3	chr19:18351400-18352000	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr19:18351600-18351800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr19:18351600-18351800	Enhancers	Colonic Mucosa	Colon
6	chr19:18351600-18351800	Flanking Active TSS	Lung	lung
7	chr19:18351600-18352000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr19:18351600-18352000	Bivalent Enhancer	Fetal Muscle Leg	muscle
9	chr19:18351600-18352000	Bivalent Enhancer	K562	blood
10	chr19:18351600-18354000	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr19:18351800-18352000	Enhancers	Lung	lung
12	chr19:18351800-18364800	Weak transcription	Colonic Mucosa	Colon
13	chr19:18352600-18352800	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr19:18352800-18353000	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr19:18352800-18363000	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr19:18353000-18362600	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr19:18353200-18362600	Weak transcription	Stomach Mucosa	stomach
18	chr19:18353400-18358800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr19:18354000-18354200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr19:18354200-18358800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr19:18358400-18359200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr19:18358400-18359200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr19:18358400-18359200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr19:18358400-18359600	Enhancers	Fetal Heart	heart
25	chr19:18358600-18358800	Bivalent Enhancer	Fetal Stomach	stomach
26	chr19:18358600-18359000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr19:18358600-18359000	Active TSS	Lung	lung
28	chr19:18358600-18359200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr19:18358600-18359200	Enhancers	H1 Cell Line	embryonic stem cell
30	chr19:18358600-18359200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr19:18358600-18359200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr19:18358800-18359000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr19:18358800-18359200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr19:18358800-18359200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr19:18358800-18359200	Enhancers	Right Ventricle	heart
36	chr19:18358800-18359400	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr19:18358800-18359600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr19:18358800-18359600	Enhancers	Fetal Stomach	stomach
39	chr19:18358800-18359600	Enhancers	K562	blood
40	chr19:18359000-18359200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr19:18359000-18359200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr19:18359000-18359200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr19:18359000-18359400	Enhancers	Lung	lung
44	chr19:18359200-18362600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr19:18359200-18362600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr19:18359200-18362800	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr19:18359600-18362600	Weak transcription	K562	blood
48	chr19:18360800-18361000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr19:18361200-18361400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
50	chr19:18361400-18375200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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