Variant report

Variant	nsv891222
Chromosome Location	chr8:100093510-100121616
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	chr8:100103092-100103687	K562	blood:	n/a	n/a
2	ATF1	chr8:100103355-100103611	K562	blood:	n/a	n/a
3	ATF2	chr8:100093166-100093626	GM12878	blood:	n/a	n/a
4	ATF2	chr8:100092901-100093701	GM12878	blood:	n/a	n/a
5	ATF3	chr8:100103253-100103550	K562	blood:	n/a	n/a
6	BATF	chr8:100093275-100093603	GM12878	blood:	n/a	n/a
7	BATF	chr8:100093290-100093609	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:100093229-100093561	GM12878	blood:	n/a	chr8:100093423-100093432
9	BCLAF1	chr8:100092916-100093613	GM12878	blood:	n/a	chr8:100093423-100093432
10	CCNT2	chr8:100103316-100103587	K562	blood:	n/a	n/a
11	CEBPB	chr8:100100423-100100719	IMR90	lung:	n/a	chr8:100100587-100100600
12	CEBPB	chr8:100101993-100102298	K562	blood:	n/a	chr8:100102138-100102149
13	CEBPB	chr8:100100439-100100639	K562	blood:	n/a	chr8:100100587-100100600
14	CEBPB	chr8:100117844-100118377	MCF-7	breast:	n/a	n/a
15	CEBPB	chr8:100102052-100102257	H1-hESC	embryonic stem cell:	n/a	chr8:100102138-100102149
16	CEBPB	chr8:100101978-100102309	A549	lung:	n/a	chr8:100102138-100102149
17	CEBPB	chr8:100101981-100102305	Hela-S3	cervix:	n/a	chr8:100102138-100102149
18	CEBPB	chr8:100101978-100102329	IMR90	lung:	n/a	chr8:100102138-100102149
19	CEBPB	chr8:100102069-100102315	HepG2	liver:	n/a	chr8:100102138-100102149
20	CEBPB	chr8:100101954-100102308	K562	blood:	n/a	chr8:100102138-100102149
21	CTCF	chr8:100103600-100103750	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr8:100112640-100112653	A549	lung:	n/a	n/a
23	CTCF	chr8:100102542-100102621	GM10248	blood:	n/a	n/a
24	CUX1	chr8:100103228-100103246	K562	blood:	n/a	n/a
25	E2F4	chr8:100104380-100104383	MCF10A-Er-Src	breast:	n/a	n/a
26	EBF1	chr8:100101249-100101395	GM12878	blood:	n/a	n/a
27	EGR1	chr8:100103155-100103480	K562	blood:	n/a	n/a
28	ELK1	chr8:100093332-100093532	GM12878	blood:	n/a	n/a
29	EP300	chr8:100117811-100118366	T-47D	breast:	n/a	n/a
30	EP300	chr8:100092951-100093594	GM12878	blood:	n/a	chr8:100093092-100093106 chr8:100093423-100093437
31	EP300	chr8:100103289-100103597	K562	blood:	n/a	n/a
32	EP300	chr8:100101778-100101856	K562	blood:	n/a	n/a
33	EP300	chr8:100093166-100093582	GM12878	blood:	n/a	chr8:100093423-100093437
34	EP300	chr8:100117937-100118290	T-47D	breast:	n/a	n/a
35	FOS	chr8:100100401-100100602	MCF10A-Er-Src	breast:	n/a	chr8:100100530-100100538 chr8:100100530-100100537 chr8:100100529-100100538 chr8:100100531-100100542
36	FOS	chr8:100100454-100100681	MCF10A-Er-Src	breast:	n/a	chr8:100100530-100100538 chr8:100100530-100100537 chr8:100100529-100100538 chr8:100100531-100100542
37	FOS	chr8:100103317-100103449	MCF10A-Er-Src	breast:	n/a	chr8:100103401-100103411 chr8:100103400-100103411 chr8:100103402-100103410 chr8:100103400-100103412 chr8:100103403-100103410
38	FOS	chr8:100103287-100103474	MCF10A-Er-Src	breast:	n/a	chr8:100103401-100103411 chr8:100103400-100103411 chr8:100103402-100103410 chr8:100103400-100103412 chr8:100103403-100103410
39	FOS	chr8:100103327-100103521	MCF10A-Er-Src	breast:	n/a	chr8:100103401-100103411 chr8:100103400-100103411 chr8:100103402-100103410 chr8:100103400-100103412 chr8:100103403-100103410
40	FOS	chr8:100103243-100103559	HUVEC	blood vessel:	n/a	chr8:100103401-100103411 chr8:100103400-100103411 chr8:100103402-100103410 chr8:100103400-100103412 chr8:100103403-100103410
41	FOS	chr8:100100381-100100708	MCF10A-Er-Src	breast:	n/a	chr8:100100530-100100538 chr8:100100530-100100537 chr8:100100529-100100538 chr8:100100531-100100542
42	FOS	chr8:100103265-100103505	MCF10A-Er-Src	breast:	n/a	chr8:100103401-100103411 chr8:100103400-100103411 chr8:100103402-100103410 chr8:100103400-100103412 chr8:100103403-100103410
43	FOS	chr8:100100434-100100656	MCF10A-Er-Src	breast:	n/a	chr8:100100530-100100538 chr8:100100530-100100537 chr8:100100529-100100538 chr8:100100531-100100542
44	FOSL1	chr8:100103220-100103482	K562	blood:	n/a	chr8:100103401-100103411 chr8:100103402-100103410 chr8:100103400-100103411 chr8:100103400-100103412 chr8:100103403-100103410
45	FOSL1	chr8:100103279-100103540	K562	blood:	n/a	chr8:100103401-100103411 chr8:100103402-100103410 chr8:100103400-100103411 chr8:100103400-100103412 chr8:100103403-100103410
46	FOSL2	chr8:100117934-100118354	MCF-7	breast:	n/a	n/a
47	FOSL2	chr8:100100372-100100668	SK-N-SH	brain:	n/a	chr8:100100530-100100538 chr8:100100530-100100537 chr8:100100529-100100538 chr8:100100531-100100542
48	FOSL2	chr8:100117801-100118291	MCF-7	breast:	n/a	n/a
49	FOXA1	chr8:100117911-100118342	T-47D	breast:	n/a	n/a
50	FOXA1	chr8:100110338-100110584	T-47D	breast:	n/a	chr8:100110489-100110504

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100104103-100104153	NH-A	brain:	n/a
2	chr8:100104103-100104153	AG10803	skin:	n/a
3	chr8:100104103-100104153	MCF-7	breast:	n/a
4	chr8:100104103-100104153	Caco-2	colon:	n/a
5	chr8:100104103-100104153	MCF10A-Er-Src	breast:	n/a
6	chr8:100104103-100104153	HMEC	breast:	n/a
7	chr8:100104103-100104153	ECC-1	luminal epithelium:	n/a
8	chr8:100104103-100104153	AG09309	skin:	n/a
9	chr8:100104103-100104153	U87	brain:	n/a
10	chr8:100104103-100104153	SKMC	muscle:	n/a
11	chr8:100104103-100104153	AG09319	gingival:	n/a
12	chr8:100104103-100104153	PrEC	prostate:	n/a
13	chr8:100104103-100104153	GM06990	blood:	n/a
14	chr8:100104103-100104153	CMK	blood:	n/a
15	chr8:100104103-100104153	NHDF-neo	bronchial:	n/a
16	chr8:100104103-100104153	HCM	heart:	n/a
17	chr8:100104103-100104153	HEEpiC	esophagus:	n/a
18	chr8:100104103-100104153	AG04450	lung:	fetal
19	chr8:100104103-100104153	H1-hESC	embryonic stem cell:	embryo
20	chr8:100104103-100104153	HAEpiC	amniotic membrane:	n/a
21	chr8:100104103-100104153	HepG2	liver:	n/a
22	chr8:100104103-100104153	GM12892	blood:	n/a
23	chr8:100104103-100104153	NHBE	bronchial:	n/a
24	chr8:100104103-100104153	HCF	heart:	n/a
25	chr8:100104103-100104153	NT2-D1	testis:	n/a
26	chr8:100104103-100104153	T-47D	breast:	n/a
27	chr8:100104103-100104153	HRCEpiC	kidney:	n/a
28	chr8:100104103-100104153	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:100104103-100104153	GM12878	blood:	n/a
30	chr8:100104103-100104153	PFSK-1	brain:	n/a
31	chr8:100104103-100104153	Hela-S3	cervix:	n/a
32	chr8:100104103-100104153	RPTEC	kidney:	n/a
33	chr8:100104103-100104153	SK-N-SH_RA	brain:	n/a
34	chr8:100104103-100104153	BJ	skin:	n/a
35	chr8:100104103-100104153	NB4	blood:	n/a
36	chr8:100104103-100104153	AG04449	skin:	fetal
37	chr8:100104103-100104153	HIPEpiC	eye:	n/a
38	chr8:100104103-100104153	LNCaP	prostate:	n/a
39	chr8:100104103-100104153	GM12891	blood:	n/a
40	chr8:100104103-100104153	A549	lung:	n/a
41	chr8:100104103-100104153	HCT-116	colon:	n/a
42	chr8:100104103-100104153	HRPEpiC	eye:	n/a
43	chr8:100104103-100104153	AoSMC	blood vessel:	n/a
44	chr8:100104103-100104153	HCPEpiC	choroid plexus:	n/a
45	chr8:100104103-100104153	SK-N-MC	brain:	n/a
46	chr8:100104103-100104153	Jurkat	blood:	n/a
47	chr8:100104103-100104153	PANC-1	pancreas:	n/a
48	chr8:100104103-100104153	HL-60	blood:	n/a
49	chr8:100104103-100104153	HEK293	kidney:	embryo
50	chr8:100104103-100104153	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:100024345..100027040-chr8:100106649..100108605,2	MCF-7	breast:
2	chr8:100024284..100027084-chr8:100113982..100120280,5	MCF-7	breast:
3	chr8:100087357..100089175-chr8:100091437..100093600,2	MCF-7	breast:
4	chr8:100109070..100113299-chr8:100115182..100118080,5	MCF-7	breast:
5	chr8:100109729..100112333-chr8:100147157..100149231,2	K562	blood:
6	chr8:100101168..100103542-chr8:100111717..100113562,2	K562	blood:
7	chr8:99955457..99958039-chr8:100115422..100117482,3	MCF-7	breast:
8	chr17:59467368..59468208-chr8:100108099..100109078,2	MCF-7	breast:
9	chr8:100024762..100026893-chr8:100106816..100109546,3	MCF-7	breast:
10	chr8:100025833..100028756-chr8:100100624..100103335,2	MCF-7	breast:
11	chr8:100101168..100103542-chr8:100111717..100113562,2	K562	blood:
12	chr8:100024034..100025700-chr8:100109623..100113452,3	MCF-7	breast:
13	chr8:99995141..99996042-chr8:100118104..100118628,2	MCF-7	breast:
14	chr8:100103552..100105106-chr8:100109674..100111736,2	K562	blood:
15	chr8:100103552..100105106-chr8:100109674..100111736,2	K562	blood:
16	chr8:100115261..100117016-chr8:100117428..100119133,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STK3-3	chr8:100106157-100106288	ENSG00000253562.1
2	lnc-STK3-3	chr8:100103966-100104326	ENSG00000253562.1

Variant related genes	Relation type
VPS13B	TF binding region
ENSG00000253562	TF binding region
VPS13B	CpG island
ENSG00000253562	CpG island
ENSG00000271930	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000164920	chromatin interactions

Extended variants
information (count: 1034 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1034 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9774546	chr8:100093510-100093511	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559289988	chr8:100093538-100093539	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs528576186	chr8:100093539-100093540	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs188116855	chr8:100093584-100093585	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs529422214	chr8:100093658-100093659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147618229	chr8:100093670-100093671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201537135	chr8:100093700-100093701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199722118	chr8:100093748-100093749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530650264	chr8:100093802-100093803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11994582	chr8:100093810-100093811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193071573	chr8:100093821-100093822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550479584	chr8:100093872-100093873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570744023	chr8:100093879-100093880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184435955	chr8:100093880-100093881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113726647	chr8:100093910-100093911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527577195	chr8:100093942-100093943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564433656	chr8:100093958-100093959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535440086	chr8:100093987-100093988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555542651	chr8:100094015-100094016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189142081	chr8:100094027-100094028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537681671	chr8:100094051-100094052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192390941	chr8:100094052-100094053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185093224	chr8:100094056-100094057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546142242	chr8:100094083-100094084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376880208	chr8:100094087-100094088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572951102	chr8:100094094-100094095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142213750	chr8:100094151-100094152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540405175	chr8:100094259-100094260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561873062	chr8:100094290-100094291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530878511	chr8:100094296-100094297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550766052	chr8:100094300-100094301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564084950	chr8:100094303-100094304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559218080	chr8:100094311-100094312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533258313	chr8:100094320-100094321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189409122	chr8:100094325-100094326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566764629	chr8:100094343-100094344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535477038	chr8:100094348-100094349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548978570	chr8:100094373-100094374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370114438	chr8:100094374-100094375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180994520	chr8:100094386-100094387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150139720	chr8:100094391-100094392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568049566	chr8:100094426-100094427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540023594	chr8:100094440-100094441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553282870	chr8:100094481-100094482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200730859	chr8:100094495-100094496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186415241	chr8:100094498-100094499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189457022	chr8:100094514-100094515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138834813	chr8:100094526-100094527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201945108	chr8:100094544-100094545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544332801	chr8:100094562-100094563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cohen syndrome	20461111	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100051400-100100400	Weak transcription	Osteobl	bone
2	chr8:100066600-100094000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr8:100078200-100103200	Weak transcription	Colon Smooth Muscle	Colon
4	chr8:100084600-100099200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:100084600-100102200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr8:100084800-100100600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr8:100088800-100100600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr8:100089800-100101000	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr8:100089800-100101400	Weak transcription	Duodenum Mucosa	Duodenum
10	chr8:100089800-100115400	Weak transcription	Left Ventricle	heart
11	chr8:100090000-100095000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr8:100090000-100115000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:100090000-100115400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr8:100090200-100118600	Weak transcription	Primary T cells from cord blood	blood
15	chr8:100090800-100126600	Weak transcription	Fetal Lung	lung
16	chr8:100091200-100115600	Weak transcription	Thymus	Thymus
17	chr8:100091200-100137000	Weak transcription	Pancreas	Pancrea
18	chr8:100091400-100116200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr8:100091600-100099400	Weak transcription	Spleen	Spleen
20	chr8:100091800-100099200	Weak transcription	Fetal Stomach	stomach
21	chr8:100092600-100093600	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr8:100092800-100093600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr8:100092800-100093600	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr8:100092800-100093600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr8:100093000-100109200	Weak transcription	Primary B cells from cord blood	blood
26	chr8:100093200-100093600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr8:100093200-100093600	Active TSS	GM12878-XiMat	blood
28	chr8:100093400-100093600	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr8:100093600-100098000	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr8:100093600-100099400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr8:100093600-100108400	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr8:100093600-100111800	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr8:100097800-100098200	ZNF genes & repeats	Fetal Muscle Leg	muscle
34	chr8:100098200-100108600	Weak transcription	Fetal Muscle Leg	muscle
35	chr8:100099200-100099600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr8:100099200-100099600	ZNF genes & repeats	Fetal Intestine Small	intestine
37	chr8:100099200-100100000	ZNF genes & repeats	Fetal Stomach	stomach
38	chr8:100099200-100160200	Weak transcription	Fetal Muscle Trunk	muscle
39	chr8:100099400-100099600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr8:100099400-100099600	Enhancers	Lung	lung
41	chr8:100099400-100099600	ZNF genes & repeats	Spleen	Spleen
42	chr8:100099600-100099800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr8:100099600-100099800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr8:100099600-100101000	Weak transcription	Fetal Intestine Small	intestine
45	chr8:100099600-100101600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr8:100099600-100108600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr8:100099600-100131400	Weak transcription	Lung	lung
48	chr8:100099600-100161000	Weak transcription	Spleen	Spleen
49	chr8:100099800-100100800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:100099800-100103800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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