Variant report

Variant	nsv1033931
Chromosome Location	chr8:19954428-19979303
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	chr8:19956978-19957083	K562	blood:	n/a	n/a
2	ATF3	chr8:19956780-19957088	K562	blood:	n/a	n/a
3	BHLHE40	chr8:19956464-19956499	K562	blood:	n/a	n/a
4	BRCA1	chr8:19971444-19971736	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr8:19963190-19963583	A549	lung:	n/a	chr8:19963393-19963402 chr8:19963391-19963402 chr8:19963391-19963404 chr8:19963393-19963404
6	CEBPB	chr8:19958612-19958942	HepG2	liver:	n/a	chr8:19958777-19958788
7	CEBPB	chr8:19958629-19958915	A549	lung:	n/a	chr8:19958777-19958788
8	CEBPB	chr8:19963208-19963576	K562	blood:	n/a	chr8:19963393-19963402 chr8:19963391-19963402 chr8:19963391-19963404 chr8:19963393-19963404
9	CEBPB	chr8:19963311-19963524	H1-hESC	embryonic stem cell:	n/a	chr8:19963393-19963402 chr8:19963391-19963402 chr8:19963391-19963404 chr8:19963393-19963404
10	CEBPB	chr8:19963199-19963613	Hela-S3	cervix:	n/a	chr8:19963393-19963402 chr8:19963391-19963402 chr8:19963391-19963404 chr8:19963393-19963404
11	CEBPB	chr8:19969333-19969623	K562	blood:	n/a	chr8:19969493-19969506 chr8:19969494-19969505 chr8:19969493-19969504 chr8:19969493-19969506
12	CEBPB	chr8:19963196-19963695	IMR90	lung:	n/a	chr8:19963393-19963402 chr8:19963391-19963402 chr8:19963391-19963404 chr8:19963393-19963404
13	CEBPB	chr8:19963303-19963448	K562	blood:	n/a	chr8:19963393-19963402 chr8:19963391-19963402 chr8:19963391-19963404 chr8:19963393-19963404
14	CEBPB	chr8:19958653-19958849	Hela-S3	cervix:	n/a	chr8:19958777-19958788
15	CEBPB	chr8:19969421-19969563	IMR90	lung:	n/a	chr8:19969493-19969506 chr8:19969494-19969505 chr8:19969493-19969504 chr8:19969493-19969506
16	CEBPB	chr8:19963277-19963562	A549	lung:	n/a	chr8:19963393-19963402 chr8:19963391-19963402 chr8:19963391-19963404 chr8:19963393-19963404
17	CEBPB	chr8:19969066-19969683	Hela-S3	cervix:	n/a	chr8:19969493-19969506 chr8:19969494-19969505 chr8:19969067-19969080 chr8:19969493-19969504 chr8:19969067-19969078 chr8:19969493-19969506
18	CEBPB	chr8:19963087-19963684	HCT-116	colon:	n/a	chr8:19963393-19963402 chr8:19963391-19963402 chr8:19963391-19963404 chr8:19963393-19963404
19	CEBPB	chr8:19963229-19963563	HepG2	liver:	n/a	chr8:19963393-19963402 chr8:19963391-19963402 chr8:19963391-19963404 chr8:19963393-19963404
20	CEBPB	chr8:19963247-19963538	HCT-116	colon:	n/a	chr8:19963393-19963402 chr8:19963391-19963402 chr8:19963391-19963404 chr8:19963393-19963404
21	CEBPB	chr8:19958624-19958942	IMR90	lung:	n/a	chr8:19958777-19958788
22	CEBPB	chr8:19969482-19969514	HepG2	liver:	n/a	chr8:19969493-19969506 chr8:19969494-19969505 chr8:19969493-19969504 chr8:19969493-19969506
23	CHD1	chr8:19966779-19966851	GM12878	blood:	n/a	n/a
24	CHD2	chr8:19960844-19961033	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr8:19963276-19963576	Hela-S3	cervix:	n/a	n/a
26	CTBP2	chr8:19960644-19961198	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:19971480-19971630	HUVEC	blood vessel:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
28	CTCF	chr8:19971487-19971710	A549	lung:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
29	CTCF	chr8:19960780-19960930	AG04450	lung:	n/a	n/a
30	CTCF	chr8:19971480-19971630	HA-sp	spinal cord:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
31	CTCF	chr8:19971358-19971706	H1-hESC	embryonic stem cell:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
32	CTCF	chr8:19971435-19971680	HepG2	liver:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
33	CTCF	chr8:19971640-19971790	GM06990	blood:	n/a	n/a
34	CTCF	chr8:19971460-19971610	HCT-116	colon:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
35	CTCF	chr8:19971480-19971630	HEEpiC	esophagus:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
36	CTCF	chr8:19971520-19971670	AG04449	skin:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
37	CTCF	chr8:19963651-19963731	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr8:19971500-19971650	AoAF	blood vessel:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
39	CTCF	chr8:19963320-19963470	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr8:19978220-19978370	GM12869	blood:	n/a	chr8:19978318-19978327
41	CTCF	chr8:19977420-19977570	NHEK	skin:	n/a	chr8:19977497-19977510
42	CTCF	chr8:19972160-19972310	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr8:19960738-19960820	K562	blood:	n/a	n/a
44	CTCF	chr8:19971500-19971650	HCPEpiC	choroid plexus:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
45	CTCF	chr8:19971476-19971662	SK-N-SH_RA	brain:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
46	CTCF	chr8:19971379-19971677	A549	lung:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
47	CTCF	chr8:19971500-19971650	HPF	lung:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
48	CTCF	chr8:19971500-19971650	HMF	breast:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
49	CTCF	chr8:19971520-19971670	HEK293	kidney:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578
50	CTCF	chr8:19971466-19971678	Medullo	brain:	n/a	chr8:19971563-19971579 chr8:19971562-19971580 chr8:19971564-19971577 chr8:19971557-19971578

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:19961386-19961436	GM06990	blood:	n/a
2	chr8:19962716-19962766	MCF10A-Er-Src	breast:	n/a
3	chr8:19961386-19961436	SK-N-SH_RA	brain:	n/a
4	chr8:19961386-19961436	BE2_C	brain:	n/a
5	chr8:19962716-19962766	GM12892	blood:	n/a
6	chr8:19961386-19961436	Hela-S3	cervix:	n/a
7	chr8:19962716-19962766	HL-60	blood:	n/a
8	chr8:19961386-19961436	T-47D	breast:	n/a
9	chr8:19961386-19961436	HMEC	breast:	n/a
10	chr8:19962716-19962766	GM12878	blood:	n/a
11	chr8:19962716-19962766	SAEC	small airway:	n/a
12	chr8:19962716-19962766	HepG2	liver:	n/a
13	chr8:19961386-19961436	HepG2	liver:	n/a
14	chr8:19961386-19961436	GM12891	blood:	n/a
15	chr8:19962716-19962766	Hepatocyte	liver:	n/a
16	chr8:19961386-19961436	Hepatocyte	liver:	n/a
17	chr8:19962716-19962766	Jurkat	blood:	n/a
18	chr8:19962716-19962766	GM12891	blood:	n/a
19	chr8:19961386-19961436	GM12892	blood:	n/a
20	chr8:19962716-19962766	SK-N-MC	brain:	n/a
21	chr8:19962716-19962766	SKMC	muscle:	n/a
22	chr8:19961386-19961436	HRCEpiC	kidney:	n/a
23	chr8:19961386-19961436	AG09309	skin:	n/a
24	chr8:19962716-19962766	Hela-S3	cervix:	n/a
25	chr8:19962716-19962766	HEK293	kidney:	embryo
26	chr8:19962716-19962766	HCT-116	colon:	n/a
27	chr8:19961386-19961436	HCT-116	colon:	n/a
28	chr8:19962716-19962766	ovcar-3	ovarian:	n/a
29	chr8:19961386-19961436	HUVEC	blood vessel:	n/a
30	chr8:19962716-19962766	Caco-2	colon:	n/a
31	chr8:19962716-19962766	HCF	heart:	n/a
32	chr8:19962716-19962766	GM06990	blood:	n/a
33	chr8:19961386-19961436	U87	brain:	n/a
34	chr8:19962716-19962766	ECC-1	luminal epithelium:	n/a
35	chr8:19962716-19962766	ProgFib	skin:	n/a
36	chr8:19961386-19961436	HL-60	blood:	n/a
37	chr8:19962716-19962766	RPTEC	kidney:	n/a
38	chr8:19962716-19962766	LNCaP	prostate:	n/a
39	chr8:19961386-19961436	ovcar-3	ovarian:	n/a
40	chr8:19961386-19961436	NHDF-neo	bronchial:	n/a
41	chr8:19961386-19961436	RPTEC	kidney:	n/a
42	chr8:19962716-19962766	PrEC	prostate:	n/a
43	chr8:19962716-19962766	NH-A	brain:	n/a
44	chr8:19962716-19962766	AG04449	skin:	fetal
45	chr8:19961386-19961436	LNCaP	prostate:	n/a
46	chr8:19962716-19962766	T-47D	breast:	n/a
47	chr8:19961386-19961436	CMK	blood:	n/a
48	chr8:19961386-19961436	PrEC	prostate:	n/a
49	chr8:19961386-19961436	AG10803	skin:	n/a
50	chr8:19961386-19961436	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:19956033..19958398-chr8:19960107..19963324,3	K562	blood:
2	chr8:19956033..19958398-chr8:19960107..19963324,3	K562	blood:
3	chr8:19946860..19949854-chr8:19953266..19956568,3	K562	blood:
4	chr8:19797802..19799354-chr8:19971667..19974269,2	K562	blood:
5	chr8:19949357..19952211-chr8:19959629..19961993,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V1B2-2	chr8:19975146-19975953	ENSG00000253775.1
2	lnc-SLC18A1-1	chr8:19970854-19971183	NONHSAT125391

Variant related genes	Relation type
RPL30P9	TF binding region
RPL30P9	CpG island

Extended variants
information (count: 1154 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1154 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565809842	chr8:19954443-19954444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147512400	chr8:19954457-19954458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369176519	chr8:19954548-19954549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551568706	chr8:19954571-19954572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185888310	chr8:19954643-19954644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537338681	chr8:19954656-19954657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549047412	chr8:19954661-19954662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73669707	chr8:19954662-19954663	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs534734471	chr8:19954666-19954667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139333725	chr8:19954717-19954718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577677908	chr8:19954755-19954756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540746924	chr8:19954769-19954770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538760316	chr8:19954780-19954781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376470768	chr8:19954788-19954789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189039271	chr8:19954801-19954802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575620379	chr8:19954884-19954885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575482318	chr8:19954915-19954916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150067677	chr8:19954925-19954926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561460298	chr8:19954944-19954945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536443714	chr8:19954963-19954964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540642390	chr8:19954969-19954970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559562440	chr8:19954971-19954972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554854050	chr8:19955000-19955001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373337219	chr8:19955037-19955038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559407427	chr8:19955050-19955051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116044394	chr8:19955074-19955075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs58717073	chr8:19955111-19955112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141626625	chr8:19955112-19955113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs398007194	chr8:19955113-19955114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10641045	chr8:19955121-19955122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7845328	chr8:19955123-19955124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540757610	chr8:19955128-19955129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181709079	chr8:19955161-19955162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565255316	chr8:19955208-19955209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563462713	chr8:19955214-19955215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530651842	chr8:19955241-19955242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148726431	chr8:19955254-19955255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567419329	chr8:19955276-19955277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200443752	chr8:19955298-19955299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186379080	chr8:19955305-19955306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544206654	chr8:19955306-19955307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533164644	chr8:19955353-19955354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113149294	chr8:19955382-19955383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545283941	chr8:19955412-19955413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530373265	chr8:19955428-19955429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376189406	chr8:19955443-19955444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113771151	chr8:19955471-19955472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140606472	chr8:19955521-19955522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145671006	chr8:19955567-19955568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373633027	chr8:19955583-19955584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
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
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
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	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
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Melanoma	20688739	CNVD
Esophageal adenocarcinoma	19417022	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19951600-19960400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr8:19952000-19961800	Weak transcription	Left Ventricle	heart
3	chr8:19956000-19956200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr8:19956000-19956200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr8:19956000-19956200	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr8:19956000-19957200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr8:19956000-19957200	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr8:19956000-19957200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr8:19956200-19956600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr8:19956200-19956600	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr8:19956200-19957200	Enhancers	Primary hematopoietic stem cells	blood
12	chr8:19956200-19957200	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr8:19956200-19957200	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr8:19956200-19957200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr8:19956200-19957400	Enhancers	Primary T cells from cord blood	blood
16	chr8:19956200-19957400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:19956200-19957600	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr8:19956200-19960400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr8:19956400-19956800	Enhancers	Primary T cells fromperipheralblood	blood
20	chr8:19956800-19957200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr8:19956800-19963400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:19957200-19960400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr8:19957200-19962800	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr8:19957200-19963200	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr8:19958200-19960400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr8:19958800-19959000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:19959000-19960600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:19959400-19959600	Enhancers	H9 Cell Line	embryonic stem cell
29	chr8:19959600-19960400	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr8:19960400-19960600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr8:19960400-19960600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr8:19960400-19961400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr8:19960400-19961600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr8:19960400-19961800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr8:19960400-19962000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr8:19960400-19962200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr8:19960400-19962200	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr8:19960400-19962200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr8:19960400-19962200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr8:19960400-19962400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr8:19960400-19963000	Enhancers	H9 Cell Line	embryonic stem cell
42	chr8:19960400-19964600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr8:19960600-19960800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr8:19960600-19960800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:19960600-19960800	Enhancers	Right Atrium	heart
46	chr8:19960600-19961000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr8:19960600-19961000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr8:19960600-19961000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr8:19960600-19961000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr8:19960600-19961000	Enhancers	Adipose Nuclei	Adipose

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