Variant report

Variant	nsv1028650
Chromosome Location	chr8:10101815-10178537
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:521)
CpG islands
(count:183)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:10131884-10131893	K562	blood:	n/a	n/a
2	ARID3A	chr8:10131468-10131733	HepG2	liver:	n/a	n/a
3	ATF2	chr8:10131302-10131671	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:10129715-10129766	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:10122977-10123170	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:10137950-10138341	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:10137958-10138346	K562	blood:	n/a	n/a
8	BATF	chr8:10176676-10176929	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:10171432-10171448	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:10131485-10131724	GM12878	blood:	n/a	n/a
11	BRCA1	chr8:10131369-10131402	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:10137032-10137545	IMR90	lung:	n/a	n/a
13	CEBPB	chr8:10137183-10137471	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:10130791-10131042	K562	blood:	n/a	n/a
15	CEBPB	chr8:10145233-10145585	IMR90	lung:	n/a	chr8:10145401-10145412
16	CEBPB	chr8:10131438-10131733	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr8:10137092-10137502	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr8:10137142-10137523	A549	lung:	n/a	n/a
19	CEBPB	chr8:10176884-10177088	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:10137106-10137442	K562	blood:	n/a	n/a
21	CEBPB	chr8:10164442-10164502	HepG2	liver:	n/a	chr8:10164448-10164459
22	CEBPB	chr8:10137072-10137500	A549	lung:	n/a	n/a
23	CEBPB	chr8:10145263-10145528	HepG2	liver:	n/a	chr8:10145401-10145412
24	CEBPB	chr8:10159793-10160252	HepG2	liver:	n/a	chr8:10159798-10159811
25	CHD2	chr8:10124773-10124838	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr8:10131400-10131759	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr8:10137070-10137507	GM12878	blood:	n/a	n/a
28	CTCF	chr8:10131446-10131709	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr8:10174380-10174530	AG04450	lung:	n/a	n/a
30	CTCF	chr8:10174460-10174610	GM12874	blood:	n/a	n/a
31	CTCF	chr8:10174340-10174490	NB4	blood:	n/a	n/a
32	CTCF	chr8:10131500-10131650	GM06990	blood:	n/a	n/a
33	CTCF	chr8:10174406-10174552	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:10174380-10174530	GM12865	blood:	n/a	n/a
35	CTCF	chr8:10174340-10174490	HAc	cerebellar:	n/a	n/a
36	CTCF	chr8:10174380-10174530	RPTEC	kidney:	n/a	n/a
37	CTCF	chr8:10131500-10131650	NHLF	lung:	n/a	n/a
38	CTCF	chr8:10131520-10131670	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr8:10131500-10131650	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr8:10131520-10131670	HVMF	connective:	n/a	n/a
41	CTCF	chr8:10131480-10131630	GM12866	blood:	n/a	n/a
42	CTCF	chr8:10131454-10131702	HepG2	liver:	n/a	n/a
43	CTCF	chr8:10174420-10174570	BE2_C	brain:	n/a	n/a
44	CTCF	chr8:10131520-10131670	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr8:10131480-10131630	NHEK	skin:	n/a	n/a
46	CTCF	chr8:10131360-10131791	GM12878	blood:	n/a	n/a
47	CTCF	chr8:10174300-10174450	RPTEC	kidney:	n/a	n/a
48	CTCF	chr8:10174219-10174646	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr8:10131480-10131630	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr8:10131430-10131701	GM19239	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10149407-10149457	CMK	blood:	n/a
2	chr8:10149407-10149457	HUVEC	blood vessel:	n/a
3	chr8:10123853-10123903	ProgFib	skin:	n/a
4	chr8:10123853-10123903	Caco-2	colon:	n/a
5	chr8:10149407-10149457	BJ	skin:	n/a
6	chr8:10123853-10123903	HMEC	breast:	n/a
7	chr8:10149407-10149457	Hela-S3	cervix:	n/a
8	chr8:10130047-10130097	Caco-2	colon:	n/a
9	chr8:10123853-10123903	NT2-D1	testis:	n/a
10	chr8:10123853-10123903	SK-N-SH_RA	brain:	n/a
11	chr8:10149407-10149457	AG09309	skin:	n/a
12	chr8:10130047-10130097	PFSK-1	brain:	n/a
13	chr8:10149407-10149457	HL-60	blood:	n/a
14	chr8:10123853-10123903	K562	blood:	n/a
15	chr8:10123853-10123903	ECC-1	luminal epithelium:	n/a
16	chr8:10130047-10130097	HMEC	breast:	n/a
17	chr8:10130047-10130097	HEK293	kidney:	embryo
18	chr8:10130047-10130097	AG04450	lung:	fetal
19	chr8:10149407-10149457	AG09319	gingival:	n/a
20	chr8:10149407-10149457	GM12892	blood:	n/a
21	chr8:10149407-10149457	K562	blood:	n/a
22	chr8:10130047-10130097	MCF10A-Er-Src	breast:	n/a
23	chr8:10123853-10123903	SK-N-MC	brain:	n/a
24	chr8:10130047-10130097	H1-hESC	embryonic stem cell:	embryo
25	chr8:10149407-10149457	GM12891	blood:	n/a
26	chr8:10130047-10130097	SKMC	muscle:	n/a
27	chr8:10130047-10130097	GM12891	blood:	n/a
28	chr8:10130047-10130097	HAEpiC	amniotic membrane:	n/a
29	chr8:10123853-10123903	HIPEpiC	eye:	n/a
30	chr8:10130047-10130097	HRPEpiC	eye:	n/a
31	chr8:10149407-10149457	GM06990	blood:	n/a
32	chr8:10123853-10123903	NHBE	bronchial:	n/a
33	chr8:10149407-10149457	SKMC	muscle:	n/a
34	chr8:10130047-10130097	A549	lung:	n/a
35	chr8:10123853-10123903	ovcar-3	ovarian:	n/a
36	chr8:10149407-10149457	PANC-1	pancreas:	n/a
37	chr8:10149407-10149457	NHBE	bronchial:	n/a
38	chr8:10130047-10130097	AG09319	gingival:	n/a
39	chr8:10149407-10149457	MCF10A-Er-Src	breast:	n/a
40	chr8:10130047-10130097	AG10803	skin:	n/a
41	chr8:10130047-10130097	GM06990	blood:	n/a
42	chr8:10149407-10149457	NT2-D1	testis:	n/a
43	chr8:10130047-10130097	HRCEpiC	kidney:	n/a
44	chr8:10123853-10123903	HCPEpiC	choroid plexus:	n/a
45	chr8:10123853-10123903	AG10803	skin:	n/a
46	chr8:10130047-10130097	NHBE	bronchial:	n/a
47	chr8:10149407-10149457	LNCaP	prostate:	n/a
48	chr8:10149407-10149457	HRE	kidney:	n/a
49	chr8:10130047-10130097	ovcar-3	ovarian:	n/a
50	chr8:10149407-10149457	HRCEpiC	kidney:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:9910082..9912394-chr8:10125398..10127467,2	MCF-7	breast:
2	chr8:9911549..9912256-chr8:10131040..10131712,2	MCF-7	breast:
3	chr8:10130155..10132980-chr8:10133293..10136060,2	MCF-7	breast:
4	chr8:10118764..10122817-chr8:10126495..10130448,3	K562	blood:
5	chr8:10178281..10180046-chr8:10185118..10187450,2	K562	blood:
6	chr8:10120963..10123282-chr8:10135840..10137757,2	K562	blood:
7	chr8:9815144..9815911-chr8:10131182..10132031,2	MCF-7	breast:
8	chr2:112640154..112641899-chr8:10166576..10168096,3	MCF-7	breast:
9	chr8:10120963..10123282-chr8:10135840..10137757,2	K562	blood:
10	chr8:9898818..9899707-chr8:10131509..10132062,2	MCF-7	breast:
11	chr8:9911202..9913645-chr8:10128676..10130785,2	MCF-7	breast:
12	chr8:10148268..10150713-chr8:10155428..10157105,2	K562	blood:
13	chr8:10118764..10122817-chr8:10126495..10130448,3	K562	blood:
14	chr8:10174620..10177509-chr8:10182842..10184423,2	K562	blood:
15	chr8:10148268..10150713-chr8:10155428..10157105,2	K562	blood:
16	chr8:10169157..10171450-chr8:10182370..10185082,2	MCF-7	breast:
17	chr8:9898835..9899700-chr8:10131105..10131973,4	MCF-7	breast:
18	chr8:10130155..10132980-chr8:10133293..10136060,2	MCF-7	breast:
19	chr8:9898892..9899783-chr8:10131113..10132044,4	K562	blood:

No data

Variant related genes	Relation type
MSRA	TF binding region
MSRA	CpG island
ENSG00000260093	chromatin interactions
ENSG00000153107	chromatin interactions
ENSG00000175806	chromatin interactions

Extended variants
information (count: 4555 )
Associated
traits (count: 136 )

Variant overlapped rSNPs/rCNVs (count:4555 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145568616	chr8:10101839-10101840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7828869	chr8:10101845-10101846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs368601039	chr8:10101891-10101892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566757164	chr8:10101901-10101902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74731945	chr8:10101911-10101912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4840468	chr8:10101914-10101915	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs575780977	chr8:10101956-10101957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538320181	chr8:10101967-10101968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2952229	chr8:10101989-10101990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74830580	chr8:10101993-10101994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568945474	chr8:10102000-10102001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574567222	chr8:10102011-10102012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142783976	chr8:10102019-10102020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185549141	chr8:10102021-10102022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143271153	chr8:10102046-10102047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551875194	chr8:10102047-10102048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7819518	chr8:10102066-10102067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs531331974	chr8:10102078-10102079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115281564	chr8:10102086-10102087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561372218	chr8:10102095-10102096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114252329	chr8:10102127-10102128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78504906	chr8:10102143-10102144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567122842	chr8:10102213-10102214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532424411	chr8:10102230-10102231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148320732	chr8:10102235-10102236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536917091	chr8:10102246-10102247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373700271	chr8:10102272-10102273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569260670	chr8:10102273-10102274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538383533	chr8:10102289-10102290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555097513	chr8:10102316-10102317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190307180	chr8:10102319-10102320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs367567904	chr8:10102327-10102328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141483800	chr8:10102333-10102334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182460366	chr8:10102343-10102344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201518369	chr8:10102383-10102384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113320351	chr8:10102410-10102411	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs545668232	chr8:10102416-10102417	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs186207620	chr8:10102435-10102436	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs376399104	chr8:10102456-10102457	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs200493833	chr8:10102457-10102458	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs112683422	chr8:10102460-10102461	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs561783694	chr8:10102514-10102515	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs530250255	chr8:10102557-10102558	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs540796167	chr8:10102566-10102567	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs529420080	chr8:10102567-10102568	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs372910520	chr8:10102569-10102570	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs559839502	chr8:10102592-10102593	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs191923908	chr8:10102610-10102611	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs375708978	chr8:10102613-10102614	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs199595787	chr8:10102618-10102619	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:136)

Disease	PMID	Source
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
Acute myeloid leukemia	21251322	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
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	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
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10060200-10103000	Weak transcription	Gastric	stomach
2	chr8:10078800-10102800	Weak transcription	Brain Germinal Matrix	brain
3	chr8:10078800-10103000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:10079200-10102600	Weak transcription	Fetal Brain Female	brain
5	chr8:10093200-10102400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:10095400-10111600	Weak transcription	Primary T cells from cord blood	blood
7	chr8:10095600-10103000	Weak transcription	Pancreas	Pancrea
8	chr8:10096000-10102600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr8:10096000-10102800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr8:10096000-10128000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr8:10096200-10107200	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr8:10096400-10102800	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr8:10097600-10103000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:10099000-10103000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr8:10099200-10102800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr8:10099200-10103000	Weak transcription	Spleen	Spleen
17	chr8:10100600-10103000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr8:10102200-10103000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:10102400-10103200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr8:10102400-10105000	Weak transcription	Fetal Brain Male	brain
21	chr8:10102600-10103000	Weak transcription	Left Ventricle	heart
22	chr8:10102600-10103000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr8:10102600-10103200	ZNF genes & repeats	Fetal Brain Female	brain
24	chr8:10102600-10103400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
25	chr8:10102800-10103000	Weak transcription	Adipose Nuclei	Adipose
26	chr8:10102800-10103200	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
27	chr8:10102800-10103400	ZNF genes & repeats	Brain Germinal Matrix	brain
28	chr8:10102800-10103600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
29	chr8:10102800-10103600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr8:10102800-10103600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr8:10102800-10103800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
32	chr8:10103000-10103200	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr8:10103000-10103200	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
34	chr8:10103000-10103200	ZNF genes & repeats	Pancreas	Pancrea
35	chr8:10103000-10103200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
36	chr8:10103000-10103400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:10103000-10103400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr8:10103000-10103400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:10103000-10103400	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
40	chr8:10103000-10103400	ZNF genes & repeats	Aorta	Aorta
41	chr8:10103000-10103400	ZNF genes & repeats	Brain Angular Gyrus	brain
42	chr8:10103000-10103400	ZNF genes & repeats	Brain Cingulate Gyrus	brain
43	chr8:10103000-10103400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
44	chr8:10103000-10103400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
45	chr8:10103000-10103400	ZNF genes & repeats	Esophagus	oesophagus
46	chr8:10103000-10103400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
47	chr8:10103000-10103400	ZNF genes & repeats	Left Ventricle	heart
48	chr8:10103000-10103400	ZNF genes & repeats	Lung	lung
49	chr8:10103000-10103400	ZNF genes & repeats	Psoas Muscle	Psoas
50	chr8:10103000-10103400	ZNF genes & repeats	Rectal Smooth Muscle	rectum

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