Variant report

Variant	esv2761450
Chromosome Location	chr8:96392380-96461950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:263)
CpG islands
(count:244)
Chromatin interactive
region (count:24)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:96398845-96399123	K562	blood:	n/a	n/a
2	BACH1	chr8:96420287-96420578	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr8:96399044-96399107	K562	blood:	n/a	n/a
4	BHLHE40	chr8:96423422-96423554	K562	blood:	n/a	chr8:96423463-96423476 chr8:96423464-96423473 chr8:96423465-96423474 chr8:96423459-96423480 chr8:96423465-96423474 chr8:96423466-96423475
5	CEBPB	chr8:96449345-96449721	HepG2	liver:	n/a	chr8:96449516-96449527
6	CEBPB	chr8:96445313-96445477	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr8:96417560-96418117	IMR90	lung:	n/a	n/a
8	CEBPB	chr8:96449382-96449610	IMR90	lung:	n/a	chr8:96449516-96449527
9	CEBPB	chr8:96449408-96449593	A549	lung:	n/a	chr8:96449516-96449527
10	CHD2	chr8:96420375-96420546	Hela-S3	cervix:	n/a	n/a
11	CTBP2	chr8:96442803-96443791	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr8:96398764-96399233	K562	blood:	n/a	n/a
13	CTCF	chr8:96398830-96399232	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr8:96398857-96399122	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr8:96443000-96443150	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr8:96413196-96413286	LNCaP	prostate:	n/a	n/a
17	CTCF	chr8:96398862-96399139	K562	blood:	n/a	n/a
18	CTCF	chr8:96399040-96399190	HCT-116	colon:	n/a	n/a
19	CTCF	chr8:96398829-96399243	HCT-116	colon:	n/a	n/a
20	CTCF	chr8:96398980-96399130	K562	blood:	n/a	n/a
21	CTCF	chr8:96398900-96399050	AG04449	skin:	n/a	n/a
22	CTCF	chr8:96398920-96399070	GM12865	blood:	n/a	n/a
23	CTCF	chr8:96398920-96399070	HCT-116	colon:	n/a	n/a
24	CTCF	chr8:96398880-96399030	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr8:96398900-96399050	HMEC	breast:	n/a	n/a
26	CTCF	chr8:96443640-96443790	HCFaa	heart:	n/a	n/a
27	CTCF	chr8:96398960-96399110	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr8:96398714-96399249	HCT-116	colon:	n/a	n/a
29	CTCF	chr8:96398920-96399070	GM12869	blood:	n/a	n/a
30	CTCF	chr8:96398920-96399070	BE2_C	brain:	n/a	n/a
31	CTCF	chr8:96398960-96399110	HEK293	kidney:	n/a	n/a
32	CTCF	chr8:96398930-96399036	GM10266	blood:	n/a	n/a
33	CTCF	chr8:96398891-96399072	NHEK	skin:	n/a	n/a
34	CTCF	chr8:96398868-96399127	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:96398840-96398990	HMEC	breast:	n/a	n/a
36	CTCF	chr8:96398823-96399165	HepG2	liver:	n/a	n/a
37	CTCF	chr8:96412980-96413130	GM12867	blood:	n/a	n/a
38	CTCF	chr8:96398893-96399078	GM19240	blood:	n/a	n/a
39	CTCF	chr8:96398880-96399030	NHEK	skin:	n/a	n/a
40	CTCF	chr8:96424000-96424150	GM12865	blood:	n/a	n/a
41	CTCF	chr8:96398920-96399070	HepG2	liver:	n/a	n/a
42	CTCF	chr8:96398940-96399090	GM12874	blood:	n/a	n/a
43	CTCF	chr8:96398860-96399010	GM12872	blood:	n/a	n/a
44	CTCF	chr8:96443120-96443270	HCM	heart:	n/a	n/a
45	CTCF	chr8:96398860-96399010	RPTEC	kidney:	n/a	n/a
46	CTCF	chr8:96398920-96399070	GM06990	blood:	n/a	n/a
47	CTCF	chr8:96398753-96399297	A549	lung:	n/a	n/a
48	CTCF	chr8:96398765-96399192	K562	blood:	n/a	n/a
49	CTCF	chr8:96398911-96399102	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr8:96398880-96399030	GM12872	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:96443153-96443203	LNCaP	prostate:	n/a
2	chr8:96393868-96393918	Jurkat	blood:	n/a
3	chr8:96443153-96443203	NHDF-neo	bronchial:	n/a
4	chr8:96393868-96393918	HRPEpiC	eye:	n/a
5	chr8:96394047-96394097	CMK	blood:	n/a
6	chr8:96418790-96418840	NH-A	brain:	n/a
7	chr8:96393868-96393918	Hela-S3	cervix:	n/a
8	chr8:96418790-96418840	HAEpiC	amniotic membrane:	n/a
9	chr8:96418790-96418840	ECC-1	luminal epithelium:	n/a
10	chr8:96443153-96443203	HCF	heart:	n/a
11	chr8:96393868-96393918	PrEC	prostate:	n/a
12	chr8:96418790-96418840	AG09319	gingival:	n/a
13	chr8:96418790-96418840	GM19239	blood:	n/a
14	chr8:96443153-96443203	BE2_C	brain:	n/a
15	chr8:96418790-96418840	NB4	blood:	n/a
16	chr8:96418790-96418840	Caco-2	colon:	n/a
17	chr8:96443153-96443203	AG10803	skin:	n/a
18	chr8:96443153-96443203	AG04450	lung:	fetal
19	chr8:96393868-96393918	T-47D	breast:	n/a
20	chr8:96418790-96418840	HRCEpiC	kidney:	n/a
21	chr8:96394047-96394097	AG09319	gingival:	n/a
22	chr8:96443153-96443203	H1-hESC	embryonic stem cell:	embryo
23	chr8:96394047-96394097	Caco-2	colon:	n/a
24	chr8:96443153-96443203	PrEC	prostate:	n/a
25	chr8:96443153-96443203	AoSMC	blood vessel:	n/a
26	chr8:96393868-96393918	GM12878	blood:	n/a
27	chr8:96443153-96443203	HIPEpiC	eye:	n/a
28	chr8:96418790-96418840	HRPEpiC	eye:	n/a
29	chr8:96443153-96443203	HL-60	blood:	n/a
30	chr8:96418790-96418840	HEEpiC	esophagus:	n/a
31	chr8:96393868-96393918	CMK	blood:	n/a
32	chr8:96418790-96418840	LNCaP	prostate:	n/a
33	chr8:96418790-96418840	H1-hESC	embryonic stem cell:	embryo
34	chr8:96394047-96394097	H1-hESC	embryonic stem cell:	embryo
35	chr8:96393868-96393918	NT2-D1	testis:	n/a
36	chr8:96393868-96393918	GM19239	blood:	n/a
37	chr8:96443153-96443203	A549	lung:	n/a
38	chr8:96418790-96418840	AG04449	skin:	fetal
39	chr8:96394047-96394097	Hela-S3	cervix:	n/a
40	chr8:96443153-96443203	Hepatocyte	liver:	n/a
41	chr8:96418790-96418840	NHBE	bronchial:	n/a
42	chr8:96393868-96393918	GM12891	blood:	n/a
43	chr8:96443153-96443203	AG09309	skin:	n/a
44	chr8:96418790-96418840	SKMC	muscle:	n/a
45	chr8:96393868-96393918	HCF	heart:	n/a
46	chr8:96394047-96394097	BE2_C	brain:	n/a
47	chr8:96418790-96418840	MCF10A-Er-Src	breast:	n/a
48	chr8:96394047-96394097	PANC-1	pancreas:	n/a
49	chr8:96393868-96393918	AoSMC	blood vessel:	n/a
50	chr8:96393868-96393918	HRE	kidney:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:96403419..96405368-chr8:96406859..96408584,2	MCF-7	breast:
2	chr8:96398409..96400158-chr8:96402287..96404999,2	K562	blood:
3	chr8:96448397..96451100-chr8:96451208..96454533,3	MCF-7	breast:
4	chr8:96403419..96405368-chr8:96406859..96408584,2	MCF-7	breast:
5	chr8:96405059..96407686-chr8:96436292..96438669,2	K562	blood:
6	chr1:121484899..121485680-chr8:96398632..96399542,2	MCF-7	breast:
7	chr8:96347218..96348000-chr8:96398502..96399465,2	MCF-7	breast:
8	chr8:96398409..96400158-chr8:96402287..96404999,2	K562	blood:
9	chr8:96430126..96432297-chr8:96457329..96459845,2	K562	blood:
10	chr8:96394533..96397301-chr8:96397590..96400549,2	K562	blood:
11	chr8:96395483..96396047-chr8:96860958..96861815,2	MCF-7	breast:
12	chr8:96405823..96408644-chr8:96412280..96414202,2	K562	blood:
13	chr8:96317394..96318355-chr8:96398480..96399433,5	MCF-7	breast:
14	chr8:96361749..96363597-chr8:96404852..96407172,2	MCF-7	breast:
15	chr8:96398658..96400358-chr8:96400929..96403787,2	K562	blood:
16	chr8:96405059..96407686-chr8:96436292..96438669,2	K562	blood:
17	chr8:96388697..96390727-chr8:96393564..96396229,2	K562	blood:
18	chr8:96430126..96432297-chr8:96457329..96459845,2	K562	blood:
19	chr8:96448397..96451100-chr8:96451208..96454533,3	MCF-7	breast:
20	chr8:96398658..96400358-chr8:96400929..96403787,2	K562	blood:
21	chr8:96394533..96397301-chr8:96397590..96400549,2	K562	blood:
22	chr8:96405823..96408644-chr8:96412280..96414202,2	K562	blood:
23	chr8:96317358..96318200-chr8:96398470..96399351,2	MCF-7	breast:
24	chr8:96410944..96413465-chr8:96415698..96417664,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHF2-2	chr8:96444854-96445008	NONHSAT127831
2	lnc-PLEKHF2-2	chr8:96444854-96445008	ENSG00000253773.1
3	lnc-PLEKHF2-2	chr8:96444865-96445008	ENSG00000253773.1
4	lnc-PLEKHF2-2	chr8:96444854-96444894	ENSG00000253773.1
5	lnc-PLEKHF2-2	chr8:96444854-96445008	NONHSAT127835
6	lnc-PLEKHF2-2	chr8:96444854-96445008	NONHSAT127837

No data

Variant related genes	Relation type
ENSG00000253945	TF binding region
ENSG00000253773	TF binding region
ENSG00000253945	CpG island
ENSG00000253773	CpG island
ENSG00000253945	chromatin interactions

Extended variants
information (count: 2207 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:2207 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141935212	chr8:96393033-96393034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568455474	chr8:96393037-96393038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537568547	chr8:96393121-96393122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116783556	chr8:96393166-96393167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569841576	chr8:96393184-96393185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538841953	chr8:96393213-96393214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78408165	chr8:96393239-96393240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572345230	chr8:96393247-96393248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2055054	chr8:96393248-96393249	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs554579067	chr8:96393261-96393262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574180896	chr8:96393304-96393305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375312220	chr8:96393317-96393318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79640693	chr8:96393359-96393360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535835831	chr8:96393423-96393424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs62522889	chr8:96393434-96393435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549056295	chr8:96393477-96393478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79352875	chr8:96393485-96393486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144340034	chr8:96393491-96393492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545996246	chr8:96393506-96393507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191206435	chr8:96393544-96393545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114259533	chr8:96393609-96393610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373151635	chr8:96393639-96393640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs3103764	chr8:96393670-96393671	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs181842640	chr8:96393693-96393694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs9297957	chr8:96393714-96393715	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs551049985	chr8:96393763-96393764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187109620	chr8:96393779-96393780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373230545	chr8:96393794-96393795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191443755	chr8:96393808-96393809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377445581	chr8:96393917-96393918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538829585	chr8:96393988-96393989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557961540	chr8:96394027-96394028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs151166365	chr8:96394042-96394043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183349640	chr8:96394162-96394163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561920904	chr8:96394204-96394205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577893034	chr8:96394214-96394215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369252908	chr8:96394215-96394216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373270038	chr8:96394251-96394252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75106316	chr8:96394292-96394293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4146363	chr8:96394316-96394317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140345610	chr8:96394348-96394349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556597559	chr8:96394351-96394352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576569681	chr8:96394360-96394361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4146362	chr8:96394361-96394362	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs535012284	chr8:96394381-96394382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150352901	chr8:96394416-96394417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144984078	chr8:96394472-96394473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs7834836	chr8:96394588-96394589	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs141139045	chr8:96394637-96394638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530888191	chr8:96394657-96394658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Malignant melanoma	17260012	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96393000-96393200	Enhancers	Left Ventricle	heart
2	chr8:96393000-96394400	Enhancers	Fetal Lung	lung
3	chr8:96393000-96394800	Enhancers	Fetal Brain Male	brain
4	chr8:96393000-96394800	Enhancers	Fetal Brain Female	brain
5	chr8:96393000-96395000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr8:96393200-96394000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr8:96393200-96394000	Enhancers	Colon Smooth Muscle	Colon
8	chr8:96393200-96394800	Enhancers	H1 Cell Line	embryonic stem cell
9	chr8:96393200-96395000	Enhancers	Fetal Stomach	stomach
10	chr8:96393600-96394000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr8:96393600-96394600	Enhancers	Brain Anterior Caudate	brain
12	chr8:96393600-96394800	Enhancers	Fetal Muscle Leg	muscle
13	chr8:96393800-96394200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr8:96393800-96394400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr8:96393800-96394400	Enhancers	Brain Hippocampus Middle	brain
16	chr8:96393800-96394400	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr8:96393800-96395400	Enhancers	Brain Germinal Matrix	brain
18	chr8:96394000-96394200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr8:96394000-96394600	Enhancers	Stomach Smooth Muscle	stomach
20	chr8:96394000-96394800	Enhancers	Brain Cingulate Gyrus	brain
21	chr8:96394000-96396200	Enhancers	Fetal Heart	heart
22	chr8:96394200-96394600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr8:96394200-96394600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr8:96394200-96394600	Enhancers	Ovary	ovary
25	chr8:96394400-96395000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr8:96394600-96398600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr8:96395000-96395400	Enhancers	Duodenum Mucosa	Duodenum
28	chr8:96395000-96395400	Enhancers	Left Ventricle	heart
29	chr8:96395000-96396200	Enhancers	Fetal Intestine Large	intestine
30	chr8:96395200-96396400	Enhancers	Fetal Intestine Small	intestine
31	chr8:96396200-96398400	Weak transcription	Fetal Heart	heart
32	chr8:96396600-96398400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr8:96398200-96398800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:96398400-96398800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr8:96398400-96398800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:96398400-96399200	Enhancers	Fetal Heart	heart
37	chr8:96398600-96399200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr8:96398800-96399800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:96399600-96400000	Active TSS	Aorta	Aorta
40	chr8:96399800-96400000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:96400000-96402600	Weak transcription	Aorta	Aorta
42	chr8:96402600-96403000	ZNF genes & repeats	Aorta	Aorta
43	chr8:96403000-96417400	Weak transcription	Aorta	Aorta
44	chr8:96405600-96406600	Enhancers	Fetal Intestine Small	intestine
45	chr8:96405800-96406200	Enhancers	Fetal Brain Female	brain
46	chr8:96405800-96406400	Enhancers	Fetal Intestine Large	intestine
47	chr8:96405800-96406400	Enhancers	Fetal Kidney	kidney
48	chr8:96406000-96406200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:96406000-96406600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr8:96406000-96406600	Enhancers	Primary hematopoietic stem cells	blood

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