Variant report

Variant	nsv1021531
Chromosome Location	chr8:6921124-7226424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1736)
CpG islands
(count:4275)
Chromatin interactive
region (count:3)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1736 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:6923929-6924081	HepG2	liver:	n/a	n/a
2	BACH1	chr8:6949393-6949420	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:7085606-7085806	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:7105978-7106319	GM12878	blood:	n/a	n/a
5	BATF	chr8:7065329-7065744	GM12878	blood:	n/a	chr8:7065585-7065596
6	BATF	chr8:7212714-7213011	GM12878	blood:	n/a	n/a
7	BATF	chr8:7065286-7065896	GM12878	blood:	n/a	chr8:7065585-7065596
8	BATF	chr8:7215669-7216199	GM12878	blood:	n/a	n/a
9	BATF	chr8:6976187-6976452	GM12878	blood:	n/a	n/a
10	BATF	chr8:7215685-7216141	GM12878	blood:	n/a	n/a
11	BATF	chr8:6976169-6976555	GM12878	blood:	n/a	n/a
12	BATF	chr8:6929911-6930147	GM12878	blood:	n/a	n/a
13	BATF	chr8:6938414-6938789	GM12878	blood:	n/a	n/a
14	BATF	chr8:7106013-7106321	GM12878	blood:	n/a	n/a
15	BATF	chr8:7016048-7016290	GM12878	blood:	n/a	n/a
16	BATF	chr8:6998432-6998646	GM12878	blood:	n/a	n/a
17	BATF	chr8:7220356-7220781	GM12878	blood:	n/a	n/a
18	BATF	chr8:6938472-6938796	GM12878	blood:	n/a	n/a
19	BCL11A	chr8:7212700-7212924	GM12878	blood:	n/a	n/a
20	BCL11A	chr8:7059717-7059897	GM12878	blood:	n/a	n/a
21	BCL11A	chr8:6975956-6976114	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:7078884-7079047	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:6963184-6963444	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:7215704-7215862	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:6963128-6963505	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:6938475-6938727	GM12878	blood:	n/a	n/a
27	BCL11A	chr8:7220370-7220830	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:7096016-7096195	GM12878	blood:	n/a	chr8:7096138-7096151
29	BCL11A	chr8:7065285-7065931	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:7213997-7214166	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:7065268-7065674	GM12878	blood:	n/a	n/a
32	BCL3	chr8:7199106-7199270	GM12878	blood:	n/a	chr8:7199138-7199147
33	BHLHE40	chr8:7212714-7213011	GM12878	blood:	n/a	n/a
34	BHLHE40	chr8:7212724-7213120	K562	blood:	n/a	n/a
35	BHLHE40	chr8:7079428-7079694	HepG2	liver:	n/a	chr8:7079551-7079567
36	BRCA1	chr8:7212733-7213463	GM12878	blood:	n/a	n/a
37	CBX3	chr8:7009532-7009840	K562	blood:	n/a	n/a
38	CEBPB	chr8:6921103-6921303	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr8:6948119-6948147	H1-hESC	embryonic stem cell:	n/a	chr8:6948133-6948142 chr8:6948131-6948144 chr8:6948132-6948143
40	CEBPB	chr8:6948092-6948185	HepG2	liver:	n/a	chr8:6948133-6948142 chr8:6948131-6948144 chr8:6948132-6948143
41	CEBPB	chr8:6990758-6990880	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr8:7178817-7179042	K562	blood:	n/a	n/a
43	CEBPB	chr8:7003837-7004114	K562	blood:	n/a	n/a
44	CEBPB	chr8:6948106-6948176	K562	blood:	n/a	chr8:6948133-6948142 chr8:6948131-6948144 chr8:6948132-6948143
45	CEBPB	chr8:7003781-7004139	K562	blood:	n/a	n/a
46	CEBPB	chr8:6990652-6990853	K562	blood:	n/a	n/a
47	CEBPB	chr8:7005971-7006346	K562	blood:	n/a	n/a
48	CEBPB	chr8:6990754-6990963	K562	blood:	n/a	n/a
49	CEBPB	chr8:7005819-7006426	K562	blood:	n/a	n/a
50	CEBPB	chr8:7216733-7216933	HepG2	liver:	n/a	chr8:7216873-7216886 chr8:7216873-7216886 chr8:7216873-7216884

(count:4275 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:7004944-7004994	GM12891	blood:	n/a
2	chr8:7005678-7005728	Hela-S3	cervix:	n/a
3	chr8:7213999-7214049	NT2-D1	testis:	n/a
4	chr8:7085602-7085652	PFSK-1	brain:	n/a
5	chr8:7079761-7079811	BE2_C	brain:	n/a
6	chr8:7004944-7004994	GM12891	blood:	n/a
7	chr8:7005678-7005728	Hela-S3	cervix:	n/a
8	chr8:7213999-7214049	NT2-D1	testis:	n/a
9	chr8:7085602-7085652	PFSK-1	brain:	n/a
10	chr8:7079761-7079811	BE2_C	brain:	n/a
11	chr8:7191953-7192003	SAEC	small airway:	n/a
12	chr8:6923300-6923350	NHBE	bronchial:	n/a
13	chr8:7079761-7079811	HCF	heart:	n/a
14	chr8:7085602-7085652	MCF10A-Er-Src	breast:	n/a
15	chr8:7005678-7005728	T-47D	breast:	n/a
16	chr8:7156743-7156793	ovcar-3	ovarian:	n/a
17	chr8:7128706-7128756	Hela-S3	cervix:	n/a
18	chr8:6932742-6932792	HRPEpiC	eye:	n/a
19	chr8:7156743-7156793	GM19239	blood:	n/a
20	chr8:6940624-6940674	HAEpiC	amniotic membrane:	n/a
21	chr8:6922705-6922755	IMR90	lung:	fetal
22	chr8:6949404-6949454	PANC-1	pancreas:	n/a
23	chr8:7154895-7154945	BE2_C	brain:	n/a
24	chr8:6940591-6940641	LNCaP	prostate:	n/a
25	chr8:6950038-6950088	ProgFib	skin:	n/a
26	chr8:7210524-7210574	Jurkat	blood:	n/a
27	chr8:7085602-7085652	Jurkat	blood:	n/a
28	chr8:7151550-7151600	HCPEpiC	choroid plexus:	n/a
29	chr8:7153685-7153735	NHDF-neo	bronchial:	n/a
30	chr8:7153685-7153735	MCF-7	breast:	n/a
31	chr8:7212700-7212750	PANC-1	pancreas:	n/a
32	chr8:6922705-6922755	Jurkat	blood:	n/a
33	chr8:7155667-7155717	RPTEC	kidney:	n/a
34	chr8:7015931-7015981	GM12891	blood:	n/a
35	chr8:7078402-7078452	K562	blood:	n/a
36	chr8:6946366-6946416	GM19239	blood:	n/a
37	chr8:7212700-7212750	AG09309	skin:	n/a
38	chr8:6931180-6931230	AG04449	skin:	fetal
39	chr8:7155225-7155275	CMK	blood:	n/a
40	chr8:7208812-7208862	Caco-2	colon:	n/a
41	chr8:7153685-7153735	HCPEpiC	choroid plexus:	n/a
42	chr8:7208812-7208862	HEK293	kidney:	embryo
43	chr8:6932644-6932694	AG09309	skin:	n/a
44	chr8:6949415-6949465	GM12878	blood:	n/a
45	chr8:7083881-7083931	SK-N-SH	brain:	n/a
46	chr8:7191953-7192003	ProgFib	skin:	n/a
47	chr8:7004819-7004869	K562	blood:	n/a
48	chr8:6950038-6950088	SK-N-MC	brain:	n/a
49	chr8:7216871-7216921	HEEpiC	esophagus:	n/a
50	chr8:7153685-7153735	Hela-S3	cervix:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:105516677..105517395-chr8:6930845..6931347,2	Hela-S3	cervix:
2	chr8:7079344..7079857-chr8:7537961..7538472,3	MCF-7	breast:
3	chr12:8332362..8333276-chr8:7212481..7212992,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB105B-3	chr8:7170368-7170425	NONHSAT124823
2	lnc-ZNF705G-1	chr8:7212333-7212511	NONHSAT124824
3	lnc-DEFB105B-4	chr8:7010239-7010328	NONHSAT124814
4	lnc-DEFB105B-3	chr8:7177268-7177473	NONHSAT124823
5	lnc-DEFB105B-4	chr8:7043806-7044422	NONHSAT124814
6	lnc-DEFA5-2	chr8:7001154-7001363	NONHSAT124813
7	lnc-ZNF705G-1	chr8:7182659-7182720	NONHSAT124824
8	lnc-ZNF705G-1	chr8:7180835-7180882	NONHSAT124824
9	lnc-ZNF705G-1	chr8:7206605-7206668	NONHSAT124824
10	lnc-ZNF705G-1	chr8:7206593-7206668	NONHSAT124826
11	lnc-ZNF705G-1	chr8:7212333-7212574	NONHSAT124826
12	lnc-ZNF705G-1	chr8:7182344-7182411	NONHSAT124824
13	lnc-ZNF705G-1	chr8:7181819-7181886	NONHSAT124824

No data

Variant related genes	Relation type
DEFB108P2	TF binding region
ENSG00000254683	TF binding region
FAM90A13P	TF binding region
FAM90A5P	TF binding region
ENSG00000216206	TF binding region
ENSG00000255273	TF binding region
ENSG00000234120	TF binding region
ZNF705G	TF binding region
FAM90A20P	TF binding region
DEFB109P1B	TF binding region
ENSG00000231930	TF binding region
ENSG00000235778	TF binding region
OR7E125P	TF binding region
ENSG00000221567	TF binding region
ENSG00000230106	TF binding region
FAM66B	TF binding region
RPS3AP30	TF binding region
ENSG00000255025	TF binding region
FAM90A3P	TF binding region
RPS3AP33	TF binding region
USP17L1P	TF binding region
USP17L4	TF binding region
FAM90A4P	TF binding region
FAM90A15P	TF binding region
DEFB108P2	CpG island
ENSG00000254683	CpG island
FAM90A13P	CpG island
FAM90A5P	CpG island
ENSG00000216206	CpG island
ENSG00000255273	CpG island
ENSG00000234120	CpG island
ZNF705G	CpG island
FAM90A20P	CpG island
DEFB109P1B	CpG island
ENSG00000231930	CpG island
ENSG00000235778	CpG island
OR7E125P	CpG island
ENSG00000221567	CpG island
ENSG00000230106	CpG island
FAM66B	CpG island
RPS3AP30	CpG island
ENSG00000255025	CpG island
FAM90A3P	CpG island
RPS3AP33	CpG island
USP17L1P	CpG island
USP17L4	CpG island
FAM90A4P	CpG island
FAM90A15P	CpG island
ENSG00000226711	chromatin interactions
ENSG00000128536	chromatin interactions
ENSG00000146776	chromatin interactions

Extended variants
information (count: 6083 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:6083 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541627488	chr8:6929205-6929206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557745462	chr8:6929214-6929215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186782183	chr8:6929215-6929216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190424443	chr8:6929216-6929217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562539593	chr8:6929223-6929224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576230394	chr8:6929230-6929231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10091747	chr8:6929237-6929238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552573375	chr8:6929248-6929249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185403095	chr8:6929254-6929255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189968542	chr8:6929273-6929274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547380447	chr8:6929275-6929276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112253994	chr8:6929288-6929289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575389589	chr8:6929305-6929306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368846283	chr8:6929312-6929313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182243422	chr8:6929330-6929331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536080813	chr8:6929338-6929339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549390155	chr8:6929342-6929343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566330345	chr8:6929360-6929361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535272989	chr8:6929365-6929366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534996289	chr8:6929368-6929369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557685739	chr8:6929381-6929382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371856995	chr8:6929391-6929392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577663495	chr8:6929393-6929394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113704022	chr8:6929400-6929401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557464821	chr8:6929408-6929409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115657257	chr8:6929418-6929419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541982351	chr8:6929425-6929426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs67655247	chr8:6929431-6929432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs73513181	chr8:6929438-6929439	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs185871349	chr8:6929443-6929444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142764673	chr8:6929460-6929461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532997530	chr8:6929463-6929464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543133930	chr8:6929471-6929472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369402133	chr8:6929478-6929479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146074630	chr8:6929485-6929486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556615825	chr8:6929486-6929487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529000862	chr8:6929490-6929491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115684822	chr8:6929496-6929497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566145538	chr8:6929508-6929509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528758341	chr8:6929528-6929529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs148720256	chr8:6929531-6929532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571294279	chr8:6929536-6929537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191419435	chr8:6929551-6929552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557100545	chr8:6929557-6929558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560786634	chr8:6929561-6929562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567713920	chr8:6929570-6929571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183459054	chr8:6929579-6929580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555489340	chr8:6929582-6929583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376030765	chr8:6930208-6930209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183610174	chr8:6930218-6930219	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:154)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
early-passage human iPS cells	21368824	CNVD
Chordoma	21215367	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	20369283	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Barrett''s syndrome	19417022	CNVD
Schizophrenia	23813976	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD

Chromatin state (count:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6929200-6929600	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr8:6930200-6930600	Enhancers	Placenta	Placenta
3	chr8:6930200-6930800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:6937000-6940000	Enhancers	Primary B cells from peripheral blood	blood
5	chr8:6937200-6940000	Enhancers	Primary B cells from cord blood	blood
6	chr8:6938400-6939400	Enhancers	GM12878-XiMat	blood
7	chr8:6940600-6940800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:6940600-6940800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:6940600-6940800	Enhancers	Spleen	Spleen
10	chr8:6944800-6945000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:6945200-6945400	Enhancers	H1 Cell Line	embryonic stem cell
12	chr8:6945200-6947000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr8:6945400-6945600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr8:6945400-6946400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr8:6945600-6945800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr8:6945600-6946600	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr8:6946000-6947200	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr8:6946200-6946400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:6946400-6946800	Enhancers	H1 Cell Line	embryonic stem cell
20	chr8:6946400-6948000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr8:6946400-6948000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:6946600-6947200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr8:6946800-6947000	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr8:6946800-6947000	Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr8:6947000-6947200	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr8:6947000-6947400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr8:6947000-6947800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr8:6947200-6947400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr8:6947200-6947400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
30	chr8:6947200-6947400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
31	chr8:6947200-6947400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr8:6947200-6947600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr8:6947200-6947600	Enhancers	H9 Cell Line	embryonic stem cell
34	chr8:6947200-6947600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:6947400-6947600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
36	chr8:6947400-6947600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
37	chr8:6947400-6947600	Enhancers	Dnd41	blood
38	chr8:6947400-6947800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr8:6947600-6948400	Weak transcription	Dnd41	blood
40	chr8:6947600-6949200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:6947600-6949600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr8:6947800-6948000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
43	chr8:6947800-6948400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
44	chr8:6948000-6948200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
45	chr8:6948000-6949400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr8:6948200-6948400	Enhancers	Spleen	Spleen
47	chr8:6948400-6949200	Weak transcription	Spleen	Spleen
48	chr8:6948400-6949200	Enhancers	Dnd41	blood
49	chr8:6949000-6949200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
50	chr8:6949000-6949200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell

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