Variant report

Variant	nsv1015637
Chromosome Location	chr8:36307431-36439165
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	ATF1	chr8:36417098-36417187	K562	blood:	n/a	n/a
2	ATF1	chr8:36378258-36378342	K562	blood:	n/a	n/a
3	BACH1	chr8:36431428-36431693	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:36431421-36431659	K562	blood:	n/a	n/a
5	CBX3	chr8:36431374-36431727	K562	blood:	n/a	n/a
6	CBX3	chr8:36431412-36431638	K562	blood:	n/a	n/a
7	CEBPB	chr8:36431375-36431729	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr8:36354356-36354687	HepG2	liver:	n/a	chr8:36354519-36354532 chr8:36354521-36354530 chr8:36354521-36354530 chr8:36354519-36354532 chr8:36354521-36354530 chr8:36354519-36354530
9	CEBPB	chr8:36311565-36311616	HepG2	liver:	n/a	n/a
10	CEBPB	chr8:36395338-36395536	HepG2	liver:	n/a	chr8:36395387-36395398
11	CEBPB	chr8:36354423-36354694	A549	lung:	n/a	chr8:36354519-36354532 chr8:36354521-36354530 chr8:36354521-36354530 chr8:36354519-36354532 chr8:36354521-36354530 chr8:36354519-36354530
12	CEBPB	chr8:36341355-36341737	H1-hESC	embryonic stem cell:	n/a	chr8:36341540-36341553 chr8:36341527-36341538
13	CEBPB	chr8:36341399-36341630	HepG2	liver:	n/a	chr8:36341540-36341553 chr8:36341527-36341538
14	CEBPB	chr8:36341413-36341687	IMR90	lung:	n/a	chr8:36341540-36341553 chr8:36341527-36341538
15	CEBPB	chr8:36354398-36354686	H1-hESC	embryonic stem cell:	n/a	chr8:36354519-36354532 chr8:36354521-36354530 chr8:36354521-36354530 chr8:36354519-36354532 chr8:36354521-36354530 chr8:36354519-36354530
16	CEBPB	chr8:36431351-36431722	MCF-7	breast:	n/a	n/a
17	CEBPB	chr8:36341380-36341685	Hela-S3	cervix:	n/a	chr8:36341540-36341553 chr8:36341527-36341538
18	CEBPB	chr8:36378883-36379028	A549	lung:	n/a	n/a
19	CEBPB	chr8:36341408-36341667	A549	lung:	n/a	chr8:36341540-36341553 chr8:36341527-36341538
20	CEBPB	chr8:36307677-36307800	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr8:36354363-36354687	IMR90	lung:	n/a	chr8:36354519-36354532 chr8:36354521-36354530 chr8:36354521-36354530 chr8:36354519-36354532 chr8:36354521-36354530 chr8:36354519-36354530
22	CEBPB	chr8:36354367-36354677	K562	blood:	n/a	chr8:36354519-36354532 chr8:36354521-36354530 chr8:36354521-36354530 chr8:36354519-36354532 chr8:36354521-36354530 chr8:36354519-36354530
23	CEBPB	chr8:36431373-36431719	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr8:36433802-36433995	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr8:36431426-36431638	A549	lung:	n/a	n/a
26	CEBPB	chr8:36431405-36431681	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr8:36431399-36431727	K562	blood:	n/a	n/a
28	CEBPD	chr8:36416869-36417294	K562	blood:	n/a	n/a
29	CHD2	chr8:36408477-36408479	GM12878	blood:	n/a	n/a
30	CHD2	chr8:36369702-36369778	K562	blood:	n/a	n/a
31	CTCF	chr8:36363280-36363430	RPTEC	kidney:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
32	CTCF	chr8:36363300-36363450	MCF-7	breast:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
33	CTCF	chr8:36363300-36363450	WERI-Rb-1	eye:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
34	CTCF	chr8:36386309-36386332	Medullo	brain:	n/a	n/a
35	CTCF	chr8:36402151-36402237	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr8:36363320-36363470	MCF-7	breast:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
37	CTCF	chr8:36363300-36363450	K562	blood:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
38	CTCF	chr8:36363260-36363410	GM12873	blood:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
39	CTCF	chr8:36363260-36363410	BE2_C	brain:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
40	CTCF	chr8:36363240-36363390	GM12871	blood:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
41	CTCF	chr8:36363300-36363450	HRPEpiC	eye:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
42	CTCF	chr8:36363360-36363510	GM12872	blood:	n/a	chr8:36363369-36363378 chr8:36363363-36363381
43	CTCF	chr8:36363260-36363410	HL-60	blood:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
44	CTCF	chr8:36377936-36378015	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:36363340-36363490	NHEK	skin:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
46	CTCF	chr8:36377961-36378003	MCF-7	breast:	n/a	n/a
47	CTCF	chr8:36363340-36363490	RPTEC	kidney:	n/a	chr8:36363358-36363379 chr8:36363369-36363378 chr8:36363363-36363381
48	CTCF	chr8:36372780-36372930	GM12869	blood:	n/a	n/a
49	CTCF	chr8:36363200-36363350	HCT-116	colon:	n/a	n/a
50	CTCF	chr8:36429600-36429750	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:36427309-36427359	K562	blood:	n/a
2	chr8:36427309-36427359	NHDF-neo	bronchial:	n/a
3	chr8:36427309-36427359	Hepatocyte	liver:	n/a
4	chr8:36427309-36427359	HEK293	kidney:	embryo
5	chr8:36427309-36427359	AG09309	skin:	n/a
6	chr8:36347870-36347920	IMR90	lung:	fetal
7	chr8:36427309-36427359	HCF	heart:	n/a
8	chr8:36380237-36380287	HIPEpiC	eye:	n/a
9	chr8:36347870-36347920	HCPEpiC	choroid plexus:	n/a
10	chr8:36427309-36427359	HCPEpiC	choroid plexus:	n/a
11	chr8:36380237-36380287	AG04450	lung:	fetal
12	chr8:36347870-36347920	HAEpiC	amniotic membrane:	n/a
13	chr8:36347870-36347920	PrEC	prostate:	n/a
14	chr8:36427309-36427359	SK-N-MC	brain:	n/a
15	chr8:36347870-36347920	HRCEpiC	kidney:	n/a
16	chr8:36347870-36347920	GM06990	blood:	n/a
17	chr8:36427309-36427359	U87	brain:	n/a
18	chr8:36347870-36347920	ovcar-3	ovarian:	n/a
19	chr8:36347870-36347920	NH-A	brain:	n/a
20	chr8:36347870-36347920	HepG2	liver:	n/a
21	chr8:36347870-36347920	K562	blood:	n/a
22	chr8:36380237-36380287	K562	blood:	n/a
23	chr8:36427309-36427359	SAEC	small airway:	n/a
24	chr8:36380237-36380287	MCF10A-Er-Src	breast:	n/a
25	chr8:36380237-36380287	PANC-1	pancreas:	n/a
26	chr8:36347870-36347920	AG04450	lung:	fetal
27	chr8:36347870-36347920	CMK	blood:	n/a
28	chr8:36347870-36347920	ECC-1	luminal epithelium:	n/a
29	chr8:36427309-36427359	HUVEC	blood vessel:	n/a
30	chr8:36347870-36347920	GM12891	blood:	n/a
31	chr8:36427309-36427359	PFSK-1	brain:	n/a
32	chr8:36380237-36380287	ovcar-3	ovarian:	n/a
33	chr8:36347870-36347920	T-47D	breast:	n/a
34	chr8:36380237-36380287	BJ	skin:	n/a
35	chr8:36427309-36427359	HL-60	blood:	n/a
36	chr8:36427309-36427359	NHBE	bronchial:	n/a
37	chr8:36427309-36427359	GM12892	blood:	n/a
38	chr8:36380237-36380287	NHBE	bronchial:	n/a
39	chr8:36427309-36427359	AG10803	skin:	n/a
40	chr8:36427309-36427359	AoSMC	blood vessel:	n/a
41	chr8:36347870-36347920	NHDF-neo	bronchial:	n/a
42	chr8:36347870-36347920	AG10803	skin:	n/a
43	chr8:36347870-36347920	HIPEpiC	eye:	n/a
44	chr8:36380237-36380287	HCM	heart:	n/a
45	chr8:36380237-36380287	SK-N-SH	brain:	n/a
46	chr8:36347870-36347920	HRE	kidney:	n/a
47	chr8:36347870-36347920	PANC-1	pancreas:	n/a
48	chr8:36347870-36347920	ProgFib	skin:	n/a
49	chr8:36347870-36347920	HCT-116	colon:	n/a
50	chr8:36380237-36380287	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:62413261..62413842-chr8:36399745..36400612,2	Hela-S3	cervix:
2	chr8:36358780..36360792-chr8:36362133..36364098,2	K562	blood:
3	chr8:36358780..36360792-chr8:36362133..36364098,2	K562	blood:
4	chr8:36395080..36396907-chr8:36399501..36401902,2	K562	blood:
5	chr8:36395080..36396907-chr8:36399501..36401902,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-419C23.1.1-3	chr8:36394909-36394994	ENSG00000253363.1
2	lnc-RP11-419C23.1.1-7	chr8:36438698-36439109	NONHSAT126019

Variant related genes	Relation type
RPL23P10	TF binding region
RPL23P10	CpG island

Extended variants
information (count: 2407 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:2407 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575812821	chr8:36307431-36307432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374145831	chr8:36307462-36307463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532587987	chr8:36307512-36307513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557891883	chr8:36307567-36307568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145195088	chr8:36307581-36307582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540226010	chr8:36307607-36307608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184909694	chr8:36307617-36307618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111260988	chr8:36307633-36307634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544517413	chr8:36307702-36307703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140831936	chr8:36307726-36307727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533161779	chr8:36307729-36307730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189754744	chr8:36307741-36307742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552204576	chr8:36307746-36307747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570607300	chr8:36307754-36307755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528602169	chr8:36307767-36307768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs10453047	chr8:36307779-36307780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546572188	chr8:36307780-36307781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12678455	chr8:36307788-36307789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565921814	chr8:36307792-36307793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568140637	chr8:36307799-36307800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535743550	chr8:36307800-36307801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148231952	chr8:36307815-36307816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78839468	chr8:36307873-36307874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141940362	chr8:36307906-36307907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150669057	chr8:36307925-36307926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558432851	chr8:36308023-36308024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539774963	chr8:36308065-36308066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572960225	chr8:36308066-36308067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191466216	chr8:36308089-36308090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555373890	chr8:36308100-36308101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183592003	chr8:36308107-36308108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551681818	chr8:36308108-36308109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544138125	chr8:36308110-36308111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562803577	chr8:36308189-36308190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577905307	chr8:36308210-36308211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189339732	chr8:36308247-36308248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569970411	chr8:36308278-36308279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181793861	chr8:36308298-36308299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs138919539	chr8:36308308-36308309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs376148499	chr8:36308328-36308329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149436598	chr8:36308332-36308333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555724780	chr8:36308345-36308346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568052028	chr8:36308377-36308378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79116372	chr8:36308379-36308380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535096369	chr8:36308381-36308382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185353427	chr8:36308414-36308415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs113687142	chr8:36308433-36308434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147448423	chr8:36308461-36308462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567092717	chr8:36308467-36308468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139856576	chr8:36308470-36308471	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	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
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
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
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	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
Seminomas	18059402	CNVD
Lung cancer	18438408	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
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	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
Multiple myeloma	16616336	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	20459607	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16912164	CNVD
Neuroticism	17667963	CNVD
Non-muscle invasive bladder neoplasm	19445696	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
Urothelial carcinoma	18382360	CNVD
Ductal carcinoma	18381933	CNVD
Breast cancer	21328542	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Intellectual disability	22045946	CNVD
Lung cancer	17925434	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	19651600	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chordoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:36303200-36308800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:36318600-36319600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:36318800-36319200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr8:36319000-36319400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr8:36331600-36333600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr8:36332600-36333600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:36332800-36334000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr8:36341600-36341800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:36347600-36348200	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr8:36347800-36348000	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr8:36348000-36348200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr8:36348000-36348400	Active TSS	NHEK	skin
13	chr8:36348200-36348400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr8:36348200-36348400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr8:36348200-36348800	Enhancers	Fetal Brain Male	brain
16	chr8:36348200-36349200	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr8:36348200-36350000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr8:36348200-36353200	Enhancers	Brain Germinal Matrix	brain
19	chr8:36348400-36348600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr8:36348400-36349200	Enhancers	Brain Angular Gyrus	brain
21	chr8:36348800-36352000	Weak transcription	Fetal Brain Male	brain
22	chr8:36350000-36351600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr8:36351600-36351800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr8:36352000-36352800	Enhancers	Fetal Brain Male	brain
25	chr8:36354000-36354200	Enhancers	Brain Cingulate Gyrus	brain
26	chr8:36357000-36358000	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr8:36358000-36359200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr8:36359200-36362600	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr8:36359400-36361600	Enhancers	Primary hematopoietic stem cells	blood
30	chr8:36360200-36362800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr8:36360400-36361000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr8:36360400-36361200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr8:36360400-36361200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:36361000-36361200	Enhancers	Brain Germinal Matrix	brain
35	chr8:36361000-36362600	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr8:36361000-36362600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr8:36361200-36362000	Weak transcription	Brain Germinal Matrix	brain
38	chr8:36361600-36362000	Weak transcription	Primary hematopoietic stem cells	blood
39	chr8:36361800-36362600	Enhancers	Fetal Brain Male	brain
40	chr8:36361800-36362600	Enhancers	Fetal Brain Female	brain
41	chr8:36362000-36362400	Enhancers	Adipose Nuclei	Adipose
42	chr8:36362000-36362400	Enhancers	Placenta Amnion	Placenta Amnion
43	chr8:36362000-36362600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr8:36362000-36362600	Enhancers	Primary hematopoietic stem cells	blood
45	chr8:36362000-36362600	Enhancers	Brain Germinal Matrix	brain
46	chr8:36362000-36362600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr8:36362000-36362600	Enhancers	Fetal Muscle Leg	muscle
48	chr8:36362200-36362600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr8:36362200-36362600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr8:36362200-36362600	Enhancers	HUES6 Cell Line	embryonic stem cell

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