Variant report

Variant	nsv831998
Chromosome Location	chr10:116847998-116969618
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	BACH1	chr10:116852386-116853318	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr10:116853916-116854116	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr10:116878147-116878431	GM12878	blood:	n/a	chr10:116878279-116878290
4	BCL11A	chr10:116966710-116966859	GM12878	blood:	n/a	n/a
5	BHLHE40	chr10:116852859-116853122	GM12878	blood:	n/a	chr10:116852939-116852955 chr10:116852927-116852943
6	BHLHE40	chr10:116852842-116853079	HepG2	liver:	n/a	chr10:116852939-116852955 chr10:116852927-116852943
7	CEBPB	chr10:116929797-116929885	HepG2	liver:	n/a	chr10:116929825-116929836
8	CEBPB	chr10:116869157-116869276	HepG2	liver:	n/a	chr10:116869164-116869175
9	CEBPB	chr10:116927494-116927774	Hela-S3	cervix:	n/a	chr10:116927673-116927684 chr10:116927632-116927643
10	CEBPB	chr10:116852024-116852345	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr10:116932005-116932101	IMR90	lung:	n/a	n/a
12	CEBPB	chr10:116927507-116927819	A549	lung:	n/a	chr10:116927673-116927684 chr10:116927632-116927643
13	CEBPB	chr10:116929771-116929965	IMR90	lung:	n/a	chr10:116929825-116929836
14	CEBPB	chr10:116927504-116927845	IMR90	lung:	n/a	chr10:116927673-116927684 chr10:116927632-116927643
15	CEBPB	chr10:116927495-116927842	HepG2	liver:	n/a	chr10:116927673-116927684 chr10:116927632-116927643
16	CEBPB	chr10:116934024-116934214	A549	lung:	n/a	n/a
17	CEBPB	chr10:116927533-116927696	K562	blood:	n/a	chr10:116927673-116927684 chr10:116927632-116927643
18	CEBPB	chr10:116934066-116934212	HepG2	liver:	n/a	n/a
19	CHD1	chr10:116852789-116853538	IMR90	lung:	n/a	chr10:116853005-116853015 chr10:116852845-116852855
20	CHD1	chr10:116852817-116853116	GM12878	blood:	n/a	chr10:116853005-116853015 chr10:116852845-116852855
21	CHD1	chr10:116852152-116853647	H1-hESC	embryonic stem cell:	n/a	chr10:116853005-116853015 chr10:116852397-116852407 chr10:116852845-116852855
22	CHD2	chr10:116852987-116853055	H1-hESC	embryonic stem cell:	n/a	chr10:116853005-116853015
23	CHD2	chr10:116852230-116852612	H1-hESC	embryonic stem cell:	n/a	chr10:116852397-116852407
24	CHD2	chr10:116852936-116852947	GM12878	blood:	n/a	n/a
25	CHD2	chr10:116853349-116853692	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTBP2	chr10:116852969-116853677	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr10:116931307-116931323	GM20000	blood:	n/a	n/a
28	CTCF	chr10:116853540-116853690	RPTEC	kidney:	n/a	n/a
29	CTCF	chr10:116931200-116931350	GM12864	blood:	n/a	chr10:116931317-116931338 chr10:116931318-116931331 chr10:116931315-116931333 chr10:116931316-116931332
30	CTCF	chr10:116853506-116853762	MCF-7	breast:	n/a	n/a
31	CTCF	chr10:116931269-116931388	Lung_OC	lung:	n/a	chr10:116931317-116931338 chr10:116931318-116931331 chr10:116931315-116931333 chr10:116931316-116931332
32	CTCF	chr10:116901020-116901387	GM12878	blood:	n/a	chr10:116901207-116901225 chr10:116901209-116901230
33	CTCF	chr10:116931260-116931410	HPAF	blood vessel:	n/a	chr10:116931317-116931338 chr10:116931318-116931331 chr10:116931315-116931333 chr10:116931316-116931332
34	CTCF	chr10:116901100-116901250	NHDF-neo	bronchial:	n/a	chr10:116901207-116901225 chr10:116901209-116901230
35	CTCF	chr10:116853560-116853710	HEK293	kidney:	n/a	n/a
36	CTCF	chr10:116901120-116901270	Caco-2	colon:	n/a	chr10:116901207-116901225 chr10:116901209-116901230
37	CTCF	chr10:116901124-116901310	Hela-S3	cervix:	n/a	chr10:116901207-116901225 chr10:116901209-116901230
38	CTCF	chr10:116889580-116889730	HMF	breast:	n/a	n/a
39	CTCF	chr10:116853560-116853710	GM12867	blood:	n/a	n/a
40	CTCF	chr10:116901135-116901286	GM10266	blood:	n/a	chr10:116901207-116901225 chr10:116901209-116901230
41	CTCF	chr10:116853487-116853733	GM13977	blood:	n/a	n/a
42	CTCF	chr10:116931360-116931510	SAEC	small airway:	n/a	n/a
43	CTCF	chr10:116901140-116901290	HMF	breast:	n/a	chr10:116901207-116901225 chr10:116901209-116901230
44	CTCF	chr10:116931268-116931385	K562	blood:	n/a	chr10:116931317-116931338 chr10:116931318-116931331 chr10:116931315-116931333 chr10:116931316-116931332
45	CTCF	chr10:116901180-116901330	HCT-116	colon:	n/a	chr10:116901207-116901225 chr10:116901209-116901230
46	CTCF	chr10:116853580-116853730	GM12872	blood:	n/a	n/a
47	CTCF	chr10:116853480-116853630	HAc	cerebellar:	n/a	n/a
48	CTCF	chr10:116901180-116901330	Caco-2	colon:	n/a	chr10:116901207-116901225 chr10:116901209-116901230
49	CTCF	chr10:116930880-116931030	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr10:116889720-116889870	AG09309	skin:	n/a	chr10:116889725-116889743 chr10:116889720-116889741

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:116852186-116852236	MCF10A-Er-Src	breast:	n/a
2	chr10:116856408-116856458	ovcar-3	ovarian:	n/a
3	chr10:116853118-116853168	HPAEpiC	pulmonary alveolar:	n/a
4	chr10:116852865-116852915	HAEpiC	amniotic membrane:	n/a
5	chr10:116853664-116853714	AG04450	lung:	fetal
6	chr10:116853468-116853518	HAEpiC	amniotic membrane:	n/a
7	chr10:116853814-116853864	HL-60	blood:	n/a
8	chr10:116853664-116853714	HRPEpiC	eye:	n/a
9	chr10:116853814-116853864	HCPEpiC	choroid plexus:	n/a
10	chr10:116853468-116853518	PrEC	prostate:	n/a
11	chr10:116853664-116853714	BE2_C	brain:	n/a
12	chr10:116853664-116853714	PFSK-1	brain:	n/a
13	chr10:116852186-116852236	HEEpiC	esophagus:	n/a
14	chr10:116853664-116853714	HNPCEpiC	eye:	n/a
15	chr10:116854028-116854078	GM12891	blood:	n/a
16	chr10:116852186-116852236	NB4	blood:	n/a
17	chr10:116852791-116852841	AG09309	skin:	n/a
18	chr10:116852186-116852236	Jurkat	blood:	n/a
19	chr10:116854499-116854549	AG10803	skin:	n/a
20	chr10:116853468-116853518	MCF-7	breast:	n/a
21	chr10:116853468-116853518	BE2_C	brain:	n/a
22	chr10:116852687-116852737	AG09309	skin:	n/a
23	chr10:116854028-116854078	ECC-1	luminal epithelium:	n/a
24	chr10:116852791-116852841	NB4	blood:	n/a
25	chr10:116852687-116852737	SK-N-MC	brain:	n/a
26	chr10:116852791-116852841	IMR90	lung:	fetal
27	chr10:116852687-116852737	GM19239	blood:	n/a
28	chr10:116849473-116849523	GM12892	blood:	n/a
29	chr10:116852470-116852520	MCF-7	breast:	n/a
30	chr10:116852470-116852520	HCT-116	colon:	n/a
31	chr10:116852470-116852520	NH-A	brain:	n/a
32	chr10:116852470-116852520	T-47D	breast:	n/a
33	chr10:116852811-116852861	HCPEpiC	choroid plexus:	n/a
34	chr10:116853468-116853518	MCF10A-Er-Src	breast:	n/a
35	chr10:116853814-116853864	HCT-116	colon:	n/a
36	chr10:116856408-116856458	NHBE	bronchial:	n/a
37	chr10:116852791-116852841	NH-A	brain:	n/a
38	chr10:116854028-116854078	IMR90	lung:	fetal
39	chr10:116852791-116852841	PFSK-1	brain:	n/a
40	chr10:116854028-116854078	MCF-7	breast:	n/a
41	chr10:116852865-116852915	GM12892	blood:	n/a
42	chr10:116853814-116853864	U87	brain:	n/a
43	chr10:116852865-116852915	MCF-7	breast:	n/a
44	chr10:116852470-116852520	Hela-S3	cervix:	n/a
45	chr10:116853814-116853864	MCF-7	breast:	n/a
46	chr10:116852687-116852737	HCF	heart:	n/a
47	chr10:116853468-116853518	K562	blood:	n/a
48	chr10:116853664-116853714	NHBE	bronchial:	n/a
49	chr10:116852470-116852520	SKMC	muscle:	n/a
50	chr10:116854028-116854078	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:116869478..116872129-chr10:116874892..116876661,2	MCF-7	breast:
2	chr10:116636495..116637116-chr10:116889645..116890541,2	MCF-7	breast:
3	chr10:116931050..116931895-chr10:117176966..117177850,3	MCF-7	breast:
4	chr10:116931581..116933131-chr10:116933638..116936531,2	MCF-7	breast:
5	chr10:116931023..116931763-chr10:117176658..117177648,2	MCF-7	breast:
6	chr10:116636491..116637413-chr10:116889245..116890241,7	MCF-7	breast:
7	chr10:116900735..116901661-chr10:117176915..117177566,4	MCF-7	breast:
8	chr10:116956281..116959165-chr10:116966788..116968734,2	MCF-7	breast:
9	chr10:116696953..116700606-chr10:116852065..116855116,4	MCF-7	breast:
10	chr10:116931581..116933131-chr10:116933638..116936531,2	MCF-7	breast:
11	chr10:116940963..116942966-chr10:116944377..116947212,2	MCF-7	breast:
12	chr10:116869478..116872129-chr10:116874892..116876661,2	MCF-7	breast:
13	chr10:116931808..116934007-chr10:116939666..116942604,2	MCF-7	breast:
14	chr10:116931808..116934007-chr10:116939666..116942604,2	MCF-7	breast:
15	chr10:116940963..116942966-chr10:116944377..116947212,2	MCF-7	breast:
16	chr10:116956281..116959165-chr10:116966788..116968734,2	MCF-7	breast:

Variant related genes	Relation type
ATRNL1	TF binding region
ATRNL1	CpG island
ENSG00000165832	chromatin interactions

Extended variants
information (count: 3544 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3544 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35699583	chr10:116848119-116848120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs180941286	chr10:116848167-116848168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150581500	chr10:116848175-116848176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139976820	chr10:116848226-116848227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11197057	chr10:116848233-116848234	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs115359615	chr10:116848263-116848264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373463663	chr10:116848283-116848284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11197058	chr10:116848289-116848290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs562126219	chr10:116848303-116848304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7089161	chr10:116848304-116848305	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs185932250	chr10:116848334-116848335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373987574	chr10:116848355-116848356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567560951	chr10:116848370-116848371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532993295	chr10:116848451-116848452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1889610	chr10:116848454-116848455	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs376010491	chr10:116848493-116848494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533510670	chr10:116848505-116848506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75075075	chr10:116848527-116848528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372700778	chr10:116848545-116848546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11197059	chr10:116848583-116848584	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs537598333	chr10:116848617-116848618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557261798	chr10:116848619-116848620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575752757	chr10:116848645-116848646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539648475	chr10:116848665-116848666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558401454	chr10:116848758-116848759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549039495	chr10:116848780-116848781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573592190	chr10:116848784-116848785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188567200	chr10:116848848-116848849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562091135	chr10:116848855-116848856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372520893	chr10:116848904-116848905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114218629	chr10:116848908-116848909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544679244	chr10:116848932-116848933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371570102	chr10:116848937-116848938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377056803	chr10:116848966-116848967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562847028	chr10:116848982-116848983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377642718	chr10:116848984-116848985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533124245	chr10:116849011-116849012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201848369	chr10:116849014-116849015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12265386	chr10:116849021-116849022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567199510	chr10:116849024-116849025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11197060	chr10:116849028-116849029	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs181358968	chr10:116849059-116849060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572164750	chr10:116849070-116849071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34391098	chr10:116849075-116849076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114370346	chr10:116849084-116849085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553878755	chr10:116849100-116849101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566966057	chr10:116849161-116849162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547159886	chr10:116849200-116849201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114997835	chr10:116849282-116849283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531446500	chr10:116849297-116849298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neuroticism	17667963	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17133270	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116845400-116851600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr10:116847200-116851000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr10:116848800-116849000	Enhancers	Fetal Brain Female	brain
4	chr10:116849200-116851000	Weak transcription	Fetal Brain Female	brain
5	chr10:116851000-116851200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr10:116851000-116851200	Enhancers	H9 Cell Line	embryonic stem cell
7	chr10:116851000-116851200	Enhancers	Fetal Brain Female	brain
8	chr10:116851000-116851600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr10:116851000-116851600	Enhancers	Rectal Smooth Muscle	rectum
10	chr10:116851000-116851800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
11	chr10:116851000-116852000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr10:116851000-116852000	Enhancers	Colon Smooth Muscle	Colon
13	chr10:116851200-116851400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr10:116851200-116851400	Enhancers	Fetal Kidney	kidney
15	chr10:116851200-116851600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
16	chr10:116851200-116851600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr10:116851200-116851800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr10:116851200-116851800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
19	chr10:116851200-116851800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
20	chr10:116851200-116851800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr10:116851200-116851800	Flanking Active TSS	Fetal Brain Female	brain
22	chr10:116851200-116851800	Enhancers	Fetal Stomach	stomach
23	chr10:116851200-116852000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr10:116851400-116851600	Enhancers	Brain Anterior Caudate	brain
25	chr10:116851400-116851600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
26	chr10:116851400-116851600	Flanking Active TSS	Fetal Kidney	kidney
27	chr10:116851400-116851800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
28	chr10:116851400-116851800	Flanking Active TSS	Brain Germinal Matrix	brain
29	chr10:116851400-116852000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
30	chr10:116851400-116852000	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
31	chr10:116851400-116853400	Active TSS	Stomach Smooth Muscle	stomach
32	chr10:116851600-116851800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
33	chr10:116851600-116851800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr10:116851600-116851800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr10:116851600-116851800	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
36	chr10:116851600-116851800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr10:116851600-116851800	Enhancers	Fetal Brain Male	brain
38	chr10:116851600-116851800	Enhancers	Fetal Kidney	kidney
39	chr10:116851600-116851800	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr10:116851600-116851800	Bivalent Enhancer	Fetal Lung	lung
41	chr10:116851600-116851800	Flanking Bivalent TSS/Enh	Rectal Smooth Muscle	rectum
42	chr10:116851600-116852000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
43	chr10:116851600-116852000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
44	chr10:116851600-116852000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr10:116851600-116852000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr10:116851600-116852000	Bivalent Enhancer	Fetal Intestine Small	intestine
47	chr10:116851600-116852200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr10:116851600-116852200	Enhancers	Placenta	Placenta
49	chr10:116851600-116852600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
50	chr10:116851600-116853200	Active TSS	Brain Cingulate Gyrus	brain

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