Variant report

Variant	nsv1026805
Chromosome Location	chr8:43144392-43786790
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1920)
CpG islands
(count:1830)
Chromatin interactive
region (count:10)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1920 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:43785555-43785668	K562	blood:	n/a	n/a
2	ATF1	chr8:43786577-43787136	K562	blood:	n/a	n/a
3	ATF3	chr8:43147119-43147233	K562	blood:	n/a	n/a
4	BACH1	chr8:43717526-43717725	K562	blood:	n/a	n/a
5	BACH1	chr8:43654724-43654750	K562	blood:	n/a	n/a
6	BACH1	chr8:43779446-43779599	K562	blood:	n/a	n/a
7	BACH1	chr8:43572418-43572443	K562	blood:	n/a	n/a
8	BATF	chr8:43761295-43761752	GM12878	blood:	n/a	n/a
9	BATF	chr8:43778905-43779151	GM12878	blood:	n/a	n/a
10	BATF	chr8:43781687-43781911	GM12878	blood:	n/a	n/a
11	BATF	chr8:43781686-43781952	GM12878	blood:	n/a	n/a
12	BATF	chr8:43785460-43785804	GM12878	blood:	n/a	n/a
13	BATF	chr8:43772038-43772467	GM12878	blood:	n/a	n/a
14	BATF	chr8:43783535-43783800	GM12878	blood:	n/a	n/a
15	BATF	chr8:43771808-43772466	GM12878	blood:	n/a	n/a
16	BATF	chr8:43776273-43776586	GM12878	blood:	n/a	n/a
17	BATF	chr8:43760193-43760718	GM12878	blood:	n/a	n/a
18	BATF	chr8:43759902-43760143	GM12878	blood:	n/a	n/a
19	BATF	chr8:43764727-43764995	GM12878	blood:	n/a	n/a
20	BATF	chr8:43785488-43786069	GM12878	blood:	n/a	n/a
21	BATF	chr8:43761208-43761764	GM12878	blood:	n/a	n/a
22	BATF	chr8:43760280-43760716	GM12878	blood:	n/a	n/a
23	BATF	chr8:43783610-43783797	GM12878	blood:	n/a	n/a
24	BATF	chr8:43760917-43761158	GM12878	blood:	n/a	n/a
25	BATF	chr8:43782910-43783364	GM12878	blood:	n/a	n/a
26	BATF	chr8:43771212-43771629	GM12878	blood:	n/a	n/a
27	BATF	chr8:43770392-43770728	GM12878	blood:	n/a	n/a
28	BATF	chr8:43771245-43771622	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:43760155-43760933	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:43772033-43772507	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:43759939-43760150	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:43778827-43779220	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:43781665-43782001	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:43771282-43771511	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:43783550-43783791	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:43785261-43786095	GM12878	blood:	n/a	n/a
37	BCL11A	chr8:43761282-43761722	GM12878	blood:	n/a	n/a
38	BCL11A	chr8:43771195-43771641	GM12878	blood:	n/a	n/a
39	BCL11A	chr8:43785511-43785821	GM12878	blood:	n/a	n/a
40	BCL11A	chr8:43783542-43783935	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:43761170-43762049	GM12878	blood:	n/a	n/a
42	BCL11A	chr8:43785334-43785462	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:43785837-43785995	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:43760267-43760707	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:43771913-43772498	GM12878	blood:	n/a	n/a
46	BCL11A	chr8:43782626-43783058	GM12878	blood:	n/a	n/a
47	BHLHE40	chr8:43768074-43768375	HepG2	liver:	n/a	n/a
48	BHLHE40	chr8:43776399-43776727	HepG2	liver:	n/a	n/a
49	BHLHE40	chr8:43781081-43781256	GM12878	blood:	n/a	n/a
50	BHLHE40	chr8:43785395-43786091	HepG2	liver:	n/a	n/a

(count:1830 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:43146218-43146268	RPTEC	kidney:	n/a
2	chr8:43405687-43405737	HIPEpiC	eye:	n/a
3	chr8:43157775-43157825	HPAEpiC	pulmonary alveolar:	n/a
4	chr8:43401874-43401924	AG04450	lung:	fetal
5	chr8:43405739-43405789	HIPEpiC	eye:	n/a
6	chr8:43147439-43147489	PANC-1	pancreas:	n/a
7	chr8:43402630-43402680	T-47D	breast:	n/a
8	chr8:43406411-43406461	HIPEpiC	eye:	n/a
9	chr8:43417050-43417100	NB4	blood:	n/a
10	chr8:43146894-43146944	Jurkat	blood:	n/a
11	chr8:43278783-43278833	Hela-S3	cervix:	n/a
12	chr8:43147554-43147604	Jurkat	blood:	n/a
13	chr8:43417050-43417100	HRE	kidney:	n/a
14	chr8:43402930-43402980	MCF-7	breast:	n/a
15	chr8:43417050-43417100	NHBE	bronchial:	n/a
16	chr8:43147439-43147489	HRPEpiC	eye:	n/a
17	chr8:43402630-43402680	SK-N-MC	brain:	n/a
18	chr8:43405687-43405737	LNCaP	prostate:	n/a
19	chr8:43405739-43405789	Hepatocyte	liver:	n/a
20	chr8:43147581-43147631	PFSK-1	brain:	n/a
21	chr8:43146894-43146944	HUVEC	blood vessel:	n/a
22	chr8:43147211-43147261	HAEpiC	amniotic membrane:	n/a
23	chr8:43275453-43275503	H1-hESC	embryonic stem cell:	embryo
24	chr8:43418406-43418456	MCF10A-Er-Src	breast:	n/a
25	chr8:43147564-43147614	MCF10A-Er-Src	breast:	n/a
26	chr8:43404458-43404508	AG09309	skin:	n/a
27	chr8:43406314-43406364	HPAEpiC	pulmonary alveolar:	n/a
28	chr8:43147602-43147652	PANC-1	pancreas:	n/a
29	chr8:43147211-43147261	HNPCEpiC	eye:	n/a
30	chr8:43147564-43147614	CMK	blood:	n/a
31	chr8:43147439-43147489	GM12878	blood:	n/a
32	chr8:43213875-43213925	Hepatocyte	liver:	n/a
33	chr8:43146388-43146438	HepG2	liver:	n/a
34	chr8:43147211-43147261	Caco-2	colon:	n/a
35	chr8:43147211-43147261	SAEC	small airway:	n/a
36	chr8:43403277-43403327	Caco-2	colon:	n/a
37	chr8:43146388-43146438	HL-60	blood:	n/a
38	chr8:43147741-43147791	MCF10A-Er-Src	breast:	n/a
39	chr8:43402930-43402980	PFSK-1	brain:	n/a
40	chr8:43147581-43147631	LNCaP	prostate:	n/a
41	chr8:43147564-43147614	HRCEpiC	kidney:	n/a
42	chr8:43147581-43147631	ovcar-3	ovarian:	n/a
43	chr8:43401874-43401924	Hepatocyte	liver:	n/a
44	chr8:43417050-43417100	GM06990	blood:	n/a
45	chr8:43405739-43405789	NT2-D1	testis:	n/a
46	chr8:43403277-43403327	NHBE	bronchial:	n/a
47	chr8:43404214-43404264	GM12892	blood:	n/a
48	chr8:43417291-43417341	HRE	kidney:	n/a
49	chr8:43147581-43147631	PANC-1	pancreas:	n/a
50	chr8:43278783-43278833	SKMC	muscle:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:42948083..42948640-chr8:43285913..43286769,2	MCF-7	breast:
2	chr8:43370024..43372377-chr8:43374871..43376951,2	K562	blood:
3	chr8:42948115..42950146-chr8:43255758..43258426,2	K562	blood:
4	chr8:43143648..43145525-chr8:43156290..43158603,2	MCF-7	breast:
5	chr5:82184309..82184963-chr8:43234719..43235395,2	MCF-7	breast:
6	chr8:43370024..43372377-chr8:43374871..43376951,2	K562	blood:
7	chr15:63385860..63386443-chr8:43553599..43554374,2	MCF-7	breast:
8	chr8:43394978..43396738-chr8:43399115..43401110,2	K562	blood:
9	chr8:42947579..42949100-chr8:43300446..43303387,2	MCF-7	breast:
10	chr8:43395245..43397661-chr8:43402500..43405220,3	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HGSNAT-12	chr8:43527966-43528218	NONHSAT126367
2	lnc-HGSNAT-6	chr8:43236787-43237091	NONHSAT126355
3	lnc-HGSNAT-7	chr8:43299491-43299558	NONHSAT126356
4	lnc-RNF170-9	chr8:43529413-43529734	NONHSAT126368
5	lnc-HGSNAT-7	chr8:43307943-43308055	NONHSAT126356
6	lnc-HGSNAT-7	chr8:43306599-43306780	NONHSAT126356
7	lnc-HGSNAT-4	chr8:43169091-43169343	NONHSAT126351
8	lnc-HGSNAT-5	chr8:43233441-43233652	NONHSAT126354
9	lnc-HGSNAT-7	chr8:43303948-43304047	NONHSAT126356
10	lnc-HGSNAT-8	chr8:43349080-43349905	NONHSAT126357
11	lnc-RNF170-8	chr8:43366963-43367176	NONHSAT126358
12	lnc-HGSNAT-10	chr8:43394280-43394615	NONHSAT126362
13	lnc-HGSNAT-7	chr8:43298045-43298224	NONHSAT126356
14	lnc-HGSNAT-9	chr8:43368786-43369564	NONHSAT126361

No data

Variant related genes	Relation type
ENSG00000253195	TF binding region
ENSG00000254145	TF binding region
ENSG00000250637	TF binding region
ENSG00000201329	TF binding region
ENSG00000254342	TF binding region
RN7SKP41	TF binding region
ENSG00000253707	TF binding region
ENSG00000264094	TF binding region
CYP4F44P	TF binding region
ENSG00000221295	TF binding region
ENSG00000253845	TF binding region
ENSG00000255497	TF binding region
ENSG00000253198	TF binding region
POTEA	TF binding region
ENSG00000253319	TF binding region
RNU6-104P	TF binding region
SNX18P27	TF binding region
ENSG00000254069	TF binding region
ENSG00000253195	CpG island
ENSG00000254145	CpG island
ENSG00000250637	CpG island
ENSG00000201329	CpG island
ENSG00000254342	CpG island
RN7SKP41	CpG island
ENSG00000253707	CpG island
ENSG00000264094	CpG island
CYP4F44P	CpG island
ENSG00000221295	CpG island
ENSG00000253845	CpG island
ENSG00000255497	CpG island
ENSG00000253198	CpG island
POTEA	CpG island
ENSG00000253319	CpG island
RNU6-104P	CpG island
SNX18P27	CpG island
ENSG00000254069	CpG island
ENSG00000185900	chromatin interactions
ENSG00000238509	chromatin interactions
ENSG00000253195	chromatin interactions
ENSG00000253748	chromatin interactions

Extended variants
information (count: 26086 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:26086 , 50 per page) page: 1 2 3 4 5 6 7 ... 522

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530702964	chr8:43144397-43144398	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs535319780	chr8:43144402-43144403	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs554763398	chr8:43144444-43144445	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs182481664	chr8:43144451-43144452	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs532607827	chr8:43144452-43144453	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs552642259	chr8:43144468-43144469	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs116712917	chr8:43144495-43144496	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs535056300	chr8:43144498-43144499	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs59693640	chr8:43144502-43144503	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs568446459	chr8:43144506-43144507	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs376896193	chr8:43144536-43144537	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537372419	chr8:43144590-43144591	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs557101280	chr8:43144610-43144611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs186483611	chr8:43144621-43144622	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs370537215	chr8:43144671-43144672	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190927232	chr8:43144674-43144675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs553079721	chr8:43144677-43144678	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs182636127	chr8:43144725-43144726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560706696	chr8:43144739-43144740	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs541837294	chr8:43144743-43144744	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs57424574	chr8:43144744-43144745	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs59827408	chr8:43144747-43144748	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs147889584	chr8:43144763-43144764	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs557141784	chr8:43144771-43144772	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564899778	chr8:43144796-43144797	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs141549800	chr8:43144797-43144798	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552377728	chr8:43144804-43144805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs566197046	chr8:43144824-43144825	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528457090	chr8:43144849-43144850	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs575217621	chr8:43144856-43144857	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs568133100	chr8:43144935-43144936	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs539549797	chr8:43144963-43144964	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs550867489	chr8:43144969-43144970	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs570707471	chr8:43145012-43145013	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569762921	chr8:43145018-43145019	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532265828	chr8:43145021-43145022	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs12677312	chr8:43145048-43145049	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs12675221	chr8:43145050-43145051	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs540066136	chr8:43145076-43145077	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs550688334	chr8:43145110-43145111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs370456715	chr8:43145111-43145112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs552770249	chr8:43145127-43145128	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572867548	chr8:43145159-43145160	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs143583295	chr8:43145160-43145161	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs560831805	chr8:43145175-43145176	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555359584	chr8:43145189-43145190	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs148065352	chr8:43145208-43145209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs376097745	chr8:43145269-43145270	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs7016102	chr8:43145298-43145299	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs141721918	chr8:43145373-43145374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
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
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	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
Colorectal cancer	16272173	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
Melanoma	18172304	CNVD
Medulloblastoma	21979893	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
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Seminomas	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21045282	CNVD
Lung cancer	17925434	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Mental retardation	17124404	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19214233	CNVD

Chromatin state (count:662 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:43142800-43148800	Weak transcription	Right Atrium	heart
2	chr8:43144000-43144600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:43146200-43148000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:43160200-43160600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:43168000-43168400	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr8:43181400-43181600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr8:43205200-43205600	Enhancers	Dnd41	blood
8	chr8:43220000-43221000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr8:43220600-43221000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:43251800-43252200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
11	chr8:43259400-43260600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr8:43261800-43264000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr8:43263000-43263600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr8:43263200-43264800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
15	chr8:43265200-43266200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:43273200-43273600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:43273800-43274000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr8:43295200-43295800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:43303200-43303800	Enhancers	Liver	Liver
20	chr8:43321800-43324400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
21	chr8:43322000-43322800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:43333000-43333600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr8:43352000-43352600	Enhancers	A549	lung
24	chr8:43352000-43353600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr8:43352200-43353000	Enhancers	Hela-S3	cervix
26	chr8:43352600-43352800	Active TSS	A549	lung
27	chr8:43352800-43353000	Flanking Active TSS	A549	lung
28	chr8:43355400-43355600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr8:43355600-43355800	Weak transcription	Aorta	Aorta
30	chr8:43359800-43360200	Enhancers	Hela-S3	cervix
31	chr8:43360000-43362600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
32	chr8:43362400-43362600	Active TSS	Spleen	Spleen
33	chr8:43362600-43367800	Weak transcription	Spleen	Spleen
34	chr8:43363800-43364000	Enhancers	Gastric	stomach
35	chr8:43364000-43368000	Weak transcription	Gastric	stomach
36	chr8:43366400-43369200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:43366600-43368600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:43367000-43368400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
39	chr8:43367800-43368200	ZNF genes & repeats	Spleen	Spleen
40	chr8:43368000-43369000	ZNF genes & repeats	Gastric	stomach
41	chr8:43368200-43369400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:43368200-43373000	Weak transcription	Spleen	Spleen
43	chr8:43371800-43373600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr8:43373000-43373600	Enhancers	Spleen	Spleen
45	chr8:43375200-43376400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr8:43377200-43380000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr8:43378400-43379600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr8:43378600-43379600	Enhancers	HepG2	liver
49	chr8:43378800-43379200	Enhancers	HMEC	breast
50	chr8:43378800-43380000	Enhancers	Left Ventricle	heart

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