Variant report

Variant	esv15264
Chromosome Location	chr14:105218866-105219411
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105219267-105219654	HepG2	liver:	n/a	chr14:105219292-105219300
2	ARID3A	chr14:105218742-105219480	K562	blood:	n/a	chr14:105219292-105219300
3	ATF1	chr14:105218785-105219664	K562	blood:	n/a	n/a
4	ATF2	chr14:105219352-105219596	GM12878	blood:	n/a	chr14:105219470-105219481
5	ATF2	chr14:105219189-105219662	GM12878	blood:	n/a	chr14:105219470-105219481
6	ATF2	chr14:105219302-105219673	H1-hESC	embryonic stem cell:	n/a	chr14:105219470-105219481
7	ATF3	chr14:105219372-105219575	GM12878	blood:	n/a	chr14:105219468-105219483 chr14:105219470-105219481 chr14:105219472-105219482 chr14:105219471-105219479 chr14:105219469-105219482 chr14:105219468-105219481 chr14:105219469-105219479 chr14:105219469-105219482 chr14:105219472-105219479 chr14:105219460-105219480 chr14:105219472-105219480 chr14:105219469-105219480 chr14:105219469-105219479 chr14:105219470-105219481 chr14:105219472-105219482
8	ATF3	chr14:105219011-105219627	K562	blood:	n/a	chr14:105219468-105219483 chr14:105219470-105219481 chr14:105219472-105219482 chr14:105219471-105219479 chr14:105219469-105219482 chr14:105219468-105219481 chr14:105219116-105219125 chr14:105219469-105219479 chr14:105219469-105219482 chr14:105219472-105219479 chr14:105219460-105219480 chr14:105219472-105219480 chr14:105219469-105219480 chr14:105219469-105219479 chr14:105219470-105219481 chr14:105219472-105219482 chr14:105219230-105219239
9	ATF3	chr14:105219156-105219698	H1-hESC	embryonic stem cell:	n/a	chr14:105219468-105219483 chr14:105219470-105219481 chr14:105219472-105219482 chr14:105219471-105219479 chr14:105219469-105219482 chr14:105219468-105219481 chr14:105219469-105219479 chr14:105219469-105219482 chr14:105219472-105219479 chr14:105219460-105219480 chr14:105219472-105219480 chr14:105219469-105219480 chr14:105219469-105219479 chr14:105219470-105219481 chr14:105219472-105219482 chr14:105219230-105219239
10	ATF3	chr14:105219336-105219651	H1-hESC	embryonic stem cell:	n/a	chr14:105219468-105219483 chr14:105219470-105219481 chr14:105219472-105219482 chr14:105219471-105219479 chr14:105219469-105219482 chr14:105219468-105219481 chr14:105219469-105219479 chr14:105219469-105219482 chr14:105219472-105219479 chr14:105219460-105219480 chr14:105219472-105219480 chr14:105219469-105219480 chr14:105219469-105219479 chr14:105219470-105219481 chr14:105219472-105219482
11	BACH1	chr14:105218992-105219687	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr14:105219283-105219556	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:105219176-105219686	K562	blood:	n/a	n/a
14	BHLHE40	chr14:105218993-105219816	GM12878	blood:	n/a	n/a
15	BRCA1	chr14:105218865-105219688	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr14:105219301-105219594	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr14:105219261-105219656	GM12878	blood:	n/a	n/a
18	BRCA1	chr14:105219287-105219703	HepG2	liver:	n/a	n/a
19	CBX3	chr14:105218261-105219139	K562	blood:	n/a	n/a
20	CBX3	chr14:105219268-105219609	K562	blood:	n/a	n/a
21	CCNT2	chr14:105218941-105219666	K562	blood:	n/a	chr14:105219195-105219204 chr14:105219116-105219125
22	CEBPB	chr14:105218942-105219619	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr14:105219349-105219531	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:105219078-105219101	K562	blood:	n/a	n/a
25	CEBPD	chr14:105218960-105219216	HepG2	liver:	n/a	n/a
26	CEBPD	chr14:105218873-105219992	HepG2	liver:	n/a	n/a
27	CEBPZ	chr14:105219279-105219485	HepG2	liver:	n/a	n/a
28	CHD2	chr14:105218780-105219664	Hela-S3	cervix:	n/a	chr14:105219108-105219118 chr14:105219210-105219220
29	CHD2	chr14:105218939-105219743	HepG2	liver:	n/a	chr14:105219108-105219118 chr14:105219210-105219220
30	CHD2	chr14:105218731-105219703	H1-hESC	embryonic stem cell:	n/a	chr14:105219108-105219118 chr14:105219210-105219220
31	CHD2	chr14:105218537-105219700	K562	blood:	n/a	chr14:105219108-105219118 chr14:105219210-105219220
32	CHD2	chr14:105218875-105219737	GM12878	blood:	n/a	chr14:105219108-105219118 chr14:105219210-105219220
33	CREB1	chr14:105218655-105221291	HepG2	liver:	n/a	chr14:105219469-105219482
34	CREB1	chr14:105218919-105219780	ECC-1	luminal epithelium:	n/a	chr14:105219469-105219482
35	CREB1	chr14:105218784-105220236	H1-hESC	embryonic stem cell:	n/a	chr14:105219469-105219482
36	CREB1	chr14:105218755-105219848	A549	lung:	n/a	chr14:105219469-105219482
37	CREB1	chr14:105218783-105219803	K562	blood:	n/a	chr14:105219469-105219482
38	CREB1	chr14:105218810-105220157	HepG2	liver:	n/a	chr14:105219469-105219482
39	CREB1	chr14:105218678-105219879	GM12878	blood:	n/a	chr14:105219469-105219482
40	CREB1	chr14:105218823-105219854	H1-hESC	embryonic stem cell:	n/a	chr14:105219469-105219482
41	CREB1	chr14:105219033-105219842	ECC-1	luminal epithelium:	n/a	chr14:105219469-105219482
42	CREB1	chr14:105218651-105219926	GM12878	blood:	n/a	chr14:105219469-105219482
43	CREB1	chr14:105218830-105219900	K562	blood:	n/a	chr14:105219469-105219482
44	CREB1	chr14:105218971-105219686	A549	lung:	n/a	chr14:105219469-105219482
45	CTCF	chr14:105218275-105218894	K562	blood:	n/a	chr14:105218540-105218553
46	CTCF	chr14:105218983-105219139	Spleen_OC	spleen:	n/a	chr14:105219119-105219129
47	CTCF	chr14:105219385-105219598	Spleen_OC	spleen:	n/a	n/a
48	E2F1	chr14:105218878-105219623	Hela-S3	cervix:	n/a	chr14:105219293-105219300 chr14:105219178-105219193 chr14:105219292-105219304 chr14:105219470-105219479 chr14:105219116-105219125 chr14:105219354-105219369 chr14:105219292-105219300 chr14:105219293-105219300 chr14:105219472-105219481 chr14:105219293-105219300 chr14:105219130-105219141
49	E2F4	chr14:105218765-105219573	GM12878	blood:	n/a	chr14:105219293-105219300 chr14:105219178-105219193 chr14:105219292-105219304 chr14:105219470-105219479 chr14:105219116-105219125 chr14:105219129-105219140 chr14:105219354-105219369 chr14:105219292-105219300 chr14:105219293-105219300 chr14:105219472-105219481 chr14:105219293-105219300
50	E2F4	chr14:105218767-105219617	Hela-S3	cervix:	n/a	chr14:105219293-105219300 chr14:105219178-105219193 chr14:105219292-105219304 chr14:105219470-105219479 chr14:105219116-105219125 chr14:105219129-105219140 chr14:105219354-105219369 chr14:105219292-105219300 chr14:105219293-105219300 chr14:105219472-105219481 chr14:105219293-105219300

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105219300-105219350	GM19239	blood:	n/a
2	chr14:105219023-105219073	BE2_C	brain:	n/a
3	chr14:105219300-105219350	NH-A	brain:	n/a
4	chr14:105219023-105219073	HRE	kidney:	n/a
5	chr14:105219230-105219280	GM12878	blood:	n/a
6	chr14:105219300-105219350	AoSMC	blood vessel:	n/a
7	chr14:105219300-105219350	AG04450	lung:	fetal
8	chr14:105219230-105219280	SAEC	small airway:	n/a
9	chr14:105219023-105219073	HNPCEpiC	eye:	n/a
10	chr14:105219230-105219280	K562	blood:	n/a
11	chr14:105219023-105219073	ProgFib	skin:	n/a
12	chr14:105219300-105219350	GM12892	blood:	n/a
13	chr14:105219023-105219073	HRCEpiC	kidney:	n/a
14	chr14:105218947-105218997	GM06990	blood:	n/a
15	chr14:105219230-105219280	ovcar-3	ovarian:	n/a
16	chr14:105218947-105218997	PANC-1	pancreas:	n/a
17	chr14:105219230-105219280	NB4	blood:	n/a
18	chr14:105219230-105219280	AoSMC	blood vessel:	n/a
19	chr14:105219300-105219350	HAEpiC	amniotic membrane:	n/a
20	chr14:105219300-105219350	U87	brain:	n/a
21	chr14:105219023-105219073	HMEC	breast:	n/a
22	chr14:105218947-105218997	NHBE	bronchial:	n/a
23	chr14:105219023-105219073	Hela-S3	cervix:	n/a
24	chr14:105219230-105219280	PFSK-1	brain:	n/a
25	chr14:105218947-105218997	ProgFib	skin:	n/a
26	chr14:105219023-105219073	NT2-D1	testis:	n/a
27	chr14:105219023-105219073	HL-60	blood:	n/a
28	chr14:105219023-105219073	GM12891	blood:	n/a
29	chr14:105219230-105219280	HNPCEpiC	eye:	n/a
30	chr14:105218947-105218997	SK-N-SH_RA	brain:	n/a
31	chr14:105219300-105219350	ECC-1	luminal epithelium:	n/a
32	chr14:105219230-105219280	U87	brain:	n/a
33	chr14:105219023-105219073	SAEC	small airway:	n/a
34	chr14:105219230-105219280	RPTEC	kidney:	n/a
35	chr14:105219023-105219073	SK-N-SH	brain:	n/a
36	chr14:105219230-105219280	BJ	skin:	n/a
37	chr14:105219300-105219350	HEEpiC	esophagus:	n/a
38	chr14:105219300-105219350	HCPEpiC	choroid plexus:	n/a
39	chr14:105218947-105218997	SAEC	small airway:	n/a
40	chr14:105219300-105219350	HIPEpiC	eye:	n/a
41	chr14:105219230-105219280	AG10803	skin:	n/a
42	chr14:105219230-105219280	NH-A	brain:	n/a
43	chr14:105219300-105219350	K562	blood:	n/a
44	chr14:105219300-105219350	GM12891	blood:	n/a
45	chr14:105218947-105218997	SK-N-MC	brain:	n/a
46	chr14:105219300-105219350	SK-N-SH	brain:	n/a
47	chr14:105219300-105219350	GM12878	blood:	n/a
48	chr14:105218947-105218997	GM12891	blood:	n/a
49	chr14:105219300-105219350	H1-hESC	embryonic stem cell:	embryo
50	chr14:105219023-105219073	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr14:105217398..105221846-chr14:105284355..105288810,4	MCF-7	breast:
2	chr14:105209075..105211830-chr14:105217895..105220741,2	K562	blood:
3	chr14:105219091..105223015-chr14:105243213..105247150,4	MCF-7	breast:
4	chr14:105217283..105220523-chr14:105237983..105243269,6	MCF-7	breast:
5	chr14:105217632..105222660-chr14:105263642..105269157,6	K562	blood:
6	chr14:105214906..105218911-chr14:105291555..105293979,3	K562	blood:
7	chr14:105218074..105222224-chr14:105239346..105242379,3	MCF-7	breast:
8	chr14:105145928..105148489-chr14:105216164..105218902,2	MCF-7	breast:
9	chr14:105141667..105144301-chr14:105219073..105221089,2	K562	blood:
10	chr14:105219309..105221110-chr14:105331526..105333449,2	MCF-7	breast:
11	chr14:105219054..105221939-chr14:105234928..105236625,2	MCF-7	breast:
12	chr14:105194869..105200156-chr14:105217139..105221997,10	K562	blood:
13	chr14:105218537..105220486-chr14:105444127..105446003,2	MCF-7	breast:
14	chr12:94853482..94854264-chr14:105218381..105219284,2	NB4	blood:
15	chr14:105172069..105174780-chr14:105216954..105219752,2	MCF-7	breast:
16	chr14:105218520..105220093-chr14:105330553..105332132,2	K562	blood:
17	chr14:105216947..105220630-chr14:105265563..105270028,6	MCF-7	breast:
18	chr14:105217901..105222027-chr14:105264438..105269623,6	K562	blood:
19	chr14:105189639..105191418-chr14:105219308..105221169,2	MCF-7	breast:
20	chr14:105219293..105222032-chr14:105260458..105263797,3	MCF-7	breast:
21	chr14:105218737..105221632-chr14:105330382..105333808,5	MCF-7	breast:
22	chr14:105218593..105220961-chr14:105330031..105332053,2	K562	blood:
23	chr1:201979602..201980181-chr14:105218934..105219572,2	Hela-S3	cervix:

Variant related genes	Relation type
SIVA1	TF binding region
SIVA1	CpG island
ENSG00000173588	chromatin interactions
ENSG00000179627	chromatin interactions
ENSG00000142208	chromatin interactions
ENSG00000258430	chromatin interactions
ENSG00000265291	chromatin interactions
ENSG00000258701	chromatin interactions
ENSG00000163435	chromatin interactions
ENSG00000256050	chromatin interactions
ENSG00000185567	chromatin interactions
ENSG00000099814	chromatin interactions
ENSG00000185100	chromatin interactions
ENSG00000203485	chromatin interactions

Extended variants
information (count: 25 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375008937	chr14:105218878-105218879	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs571887610	chr14:105218881-105218882	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs537517692	chr14:105218893-105218894	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs541834925	chr14:105218930-105218931	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs557497676	chr14:105218966-105218967	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs574042672	chr14:105219063-105219064	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs3809454	chr14:105219069-105219070	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs561005335	chr14:105219077-105219078	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs576667443	chr14:105219101-105219102	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs144648740	chr14:105219123-105219124	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs148480125	chr14:105219124-105219125	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs59165659	chr14:105219180-105219181	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs544989195	chr14:105219233-105219234	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs558301675	chr14:105219282-105219283	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs575098428	chr14:105219289-105219290	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs543864179	chr14:105219302-105219303	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs147187633	chr14:105219309-105219310	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs60829853	chr14:105219310-105219311	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs572341329	chr14:105219313-105219314	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs547707805	chr14:105219338-105219339	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs540248736	chr14:105219362-105219363	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs140478039	chr14:105219371-105219372	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs187255160	chr14:105219385-105219386	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs190830644	chr14:105219398-105219399	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
25	rs61493636	chr14:105219403-105219404	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	20932292	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105204200-105219600	Weak transcription	Fetal Heart	heart
2	chr14:105218200-105219000	Flanking Active TSS	Dnd41	blood
3	chr14:105218200-105219000	Flanking Active TSS	HepG2	liver
4	chr14:105218200-105219600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr14:105218200-105220600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr14:105218400-105219000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr14:105218400-105219000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr14:105218400-105219000	Flanking Active TSS	Primary B cells from peripheral blood	blood
9	chr14:105218400-105219000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
10	chr14:105218400-105219000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
11	chr14:105218400-105219000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
12	chr14:105218400-105219000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr14:105218400-105219000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
14	chr14:105218400-105219000	Flanking Active TSS	Adipose Nuclei	Adipose
15	chr14:105218400-105219000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr14:105218400-105219000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
17	chr14:105218400-105219000	Flanking Active TSS	Fetal Intestine Small	intestine
18	chr14:105218400-105219000	Flanking Active TSS	Placenta	Placenta
19	chr14:105218400-105219000	Flanking Active TSS	Fetal Thymus	thymus
20	chr14:105218400-105219000	Flanking Active TSS	Rectal Smooth Muscle	rectum
21	chr14:105218400-105219000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
22	chr14:105218400-105219000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
23	chr14:105218400-105219000	Flanking Active TSS	Hela-S3	cervix
24	chr14:105218400-105219000	Flanking Active TSS	HMEC	breast
25	chr14:105218400-105220000	Active TSS	Primary T cells from cord blood	blood
26	chr14:105218400-105220200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr14:105218400-105220200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr14:105218400-105220200	Active TSS	Primary T killer memory cells from peripheral blood	blood
29	chr14:105218400-105220200	Active TSS	Brain Substantia Nigra	brain
30	chr14:105218400-105220200	Active TSS	K562	blood
31	chr14:105218400-105220200	Active TSS	NHEK	skin
32	chr14:105218400-105220400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr14:105218400-105220400	Active TSS	iPS-18 Cell Line	embryonic stem cell
34	chr14:105218400-105220400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr14:105218400-105220400	Active TSS	HSMM	muscle
36	chr14:105218400-105220600	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr14:105218400-105221000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr14:105218400-105221000	Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr14:105218600-105219000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
40	chr14:105218600-105219000	Flanking Active TSS	Liver	Liver
41	chr14:105218600-105219000	Flanking Active TSS	Fetal Brain Male	brain
42	chr14:105218600-105219000	Flanking Active TSS	Fetal Intestine Large	intestine
43	chr14:105218600-105219000	Flanking Active TSS	Fetal Lung	lung
44	chr14:105218600-105219000	Flanking Active TSS	Fetal Muscle Trunk	muscle
45	chr14:105218600-105219000	Flanking Active TSS	Osteobl	bone
46	chr14:105218600-105220200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr14:105218600-105220200	Active TSS	H1 Cell Line	embryonic stem cell
48	chr14:105218600-105220200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr14:105218600-105220200	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr14:105218600-105220200	Active TSS	Ovary	ovary

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