Variant report

Variant	esv3334079
Chromosome Location	chr1:215717606-215745691
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:765)
CpG islands
(count:614)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:765 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:215742767-215743420	K562	blood:	n/a	n/a
2	ARID3A	chr1:215740376-215740690	K562	blood:	n/a	n/a
3	ARID3A	chr1:215742821-215743217	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:215740265-215740878	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:215731313-215731767	HepG2	liver:	n/a	n/a
6	BACH1	chr1:215740321-215740761	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:215740222-215740685	K562	blood:	n/a	n/a
8	BACH1	chr1:215741172-215741269	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr1:215740317-215740899	A549	lung:	n/a	chr1:215740719-215740732 chr1:215740865-215740878 chr1:215740885-215740894
10	BCLAF1	chr1:215740328-215740960	K562	blood:	n/a	chr1:215740719-215740732 chr1:215740865-215740878 chr1:215740885-215740894
11	BCLAF1	chr1:215740366-215741262	GM12878	blood:	n/a	chr1:215740719-215740732 chr1:215740865-215740878 chr1:215741130-215741143 chr1:215740885-215740894
12	BHLHE40	chr1:215740115-215741532	K562	blood:	n/a	chr1:215740964-215740980
13	BHLHE40	chr1:215740502-215741201	GM12878	blood:	n/a	chr1:215740964-215740980
14	BRCA1	chr1:215721111-215721310	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr1:215740073-215740146	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr1:215740383-215740558	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr1:215742934-215744103	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr1:215740296-215740719	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr1:215733994-215734308	K562	blood:	n/a	n/a
20	CBX3	chr1:215728884-215729225	K562	blood:	n/a	n/a
21	CBX3	chr1:215741077-215741619	K562	blood:	n/a	n/a
22	CBX3	chr1:215740281-215740949	K562	blood:	n/a	n/a
23	CBX3	chr1:215742181-215743187	K562	blood:	n/a	n/a
24	CBX3	chr1:215728870-215729255	K562	blood:	n/a	n/a
25	CCNT2	chr1:215740373-215741290	K562	blood:	n/a	n/a
26	CEBPB	chr1:215741097-215741591	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:215740197-215740562	A549	lung:	n/a	n/a
28	CEBPB	chr1:215740367-215740700	K562	blood:	n/a	n/a
29	CEBPB	chr1:215732852-215733011	K562	blood:	n/a	n/a
30	CEBPB	chr1:215725518-215725587	A549	lung:	n/a	n/a
31	CEBPB	chr1:215740158-215740868	MCF-7	breast:	n/a	n/a
32	CEBPB	chr1:215740527-215740802	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr1:215740060-215740887	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr1:215741235-215741591	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr1:215741018-215741094	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPD	chr1:215740378-215741077	HepG2	liver:	n/a	n/a
37	CHD1	chr1:215739972-215741689	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr1:215741048-215741499	GM12878	blood:	n/a	n/a
39	CHD1	chr1:215742064-215742237	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr1:215740425-215740829	HepG2	liver:	n/a	n/a
41	CHD2	chr1:215740304-215740768	GM12878	blood:	n/a	n/a
42	CHD2	chr1:215740381-215740711	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr1:215741109-215741309	GM12878	blood:	n/a	n/a
44	CHD2	chr1:215741123-215741327	HepG2	liver:	n/a	n/a
45	CHD2	chr1:215740354-215741584	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr1:215741101-215741334	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr1:215740378-215741620	K562	blood:	n/a	n/a
48	CHD2	chr1:215730343-215730519	HepG2	liver:	n/a	n/a
49	CREB1	chr1:215740259-215741593	HepG2	liver:	n/a	n/a
50	CREB1	chr1:215740357-215741136	A549	lung:	n/a	n/a

(count:614 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:215740697-215740747	GM12891	blood:	n/a
2	chr1:215740701-215740751	HRPEpiC	eye:	n/a
3	chr1:215737048-215737098	GM06990	blood:	n/a
4	chr1:215740424-215740474	HRCEpiC	kidney:	n/a
5	chr1:215740697-215740747	GM12891	blood:	n/a
6	chr1:215740701-215740751	HRPEpiC	eye:	n/a
7	chr1:215737048-215737098	GM06990	blood:	n/a
8	chr1:215740424-215740474	HRCEpiC	kidney:	n/a
9	chr1:215745036-215745086	Hela-S3	cervix:	n/a
10	chr1:215741258-215741308	HL-60	blood:	n/a
11	chr1:215741182-215741232	HepG2	liver:	n/a
12	chr1:215745036-215745086	RPTEC	kidney:	n/a
13	chr1:215741182-215741232	AoSMC	blood vessel:	n/a
14	chr1:215737048-215737098	NHBE	bronchial:	n/a
15	chr1:215737048-215737098	GM12892	blood:	n/a
16	chr1:215741843-215741893	GM12892	blood:	n/a
17	chr1:215745036-215745086	PFSK-1	brain:	n/a
18	chr1:215741182-215741232	T-47D	breast:	n/a
19	chr1:215741318-215741368	HMEC	breast:	n/a
20	chr1:215740424-215740474	AoSMC	blood vessel:	n/a
21	chr1:215741318-215741368	AG04449	skin:	fetal
22	chr1:215740697-215740747	A549	lung:	n/a
23	chr1:215740071-215740121	H1-hESC	embryonic stem cell:	embryo
24	chr1:215740424-215740474	ProgFib	skin:	n/a
25	chr1:215741182-215741232	Jurkat	blood:	n/a
26	chr1:215741843-215741893	HRE	kidney:	n/a
27	chr1:215741843-215741893	HCM	heart:	n/a
28	chr1:215740424-215740474	HMEC	breast:	n/a
29	chr1:215740424-215740474	SK-N-SH_RA	brain:	n/a
30	chr1:215740701-215740751	HepG2	liver:	n/a
31	chr1:215737048-215737098	HRPEpiC	eye:	n/a
32	chr1:215741182-215741232	GM19239	blood:	n/a
33	chr1:215740424-215740474	HEK293	kidney:	embryo
34	chr1:215740697-215740747	NHDF-neo	bronchial:	n/a
35	chr1:215740697-215740747	GM12878	blood:	n/a
36	chr1:215740071-215740121	AG10803	skin:	n/a
37	chr1:215745036-215745086	ProgFib	skin:	n/a
38	chr1:215740701-215740751	GM06990	blood:	n/a
39	chr1:215745036-215745086	GM12892	blood:	n/a
40	chr1:215737048-215737098	AG04449	skin:	fetal
41	chr1:215740701-215740751	NHBE	bronchial:	n/a
42	chr1:215737048-215737098	Hela-S3	cervix:	n/a
43	chr1:215740071-215740121	AG09309	skin:	n/a
44	chr1:215745036-215745086	U87	brain:	n/a
45	chr1:215740071-215740121	BJ	skin:	n/a
46	chr1:215741318-215741368	SAEC	small airway:	n/a
47	chr1:215745036-215745086	SAEC	small airway:	n/a
48	chr1:215741843-215741893	HMEC	breast:	n/a
49	chr1:215741318-215741368	SK-N-MC	brain:	n/a
50	chr1:215741182-215741232	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:215740857..215741766-chr12:7052939..7053914,2	Hela-S3	cervix:
2	chr1:215735916..215738873-chr1:215738967..215741974,4	MCF-7	breast:
3	chr1:215729059..215730729-chr1:215736109..215738919,2	MCF-7	breast:
4	chr1:215739388..215743068-chr1:215745972..215749293,5	MCF-7	breast:
5	chr1:215732968..215735499-chr1:215739364..215742165,4	MCF-7	breast:
6	chr1:215727802..215730014-chr1:215737556..215740283,2	K562	blood:
7	chr1:215742124..215744108-chr1:215859791..215861523,2	K562	blood:
8	chr1:215731051..215732589-chr1:215739123..215741939,2	MCF-7	breast:
9	chr1:215718496..215720254-chr1:215739655..215742103,3	MCF-7	breast:
10	chr1:215722423..215724891-chr1:215740211..215742928,2	K562	blood:
11	chr1:215728115..215729776-chr1:215731286..215732796,2	MCF-7	breast:
12	chr1:215728115..215729776-chr1:215731286..215732796,2	MCF-7	breast:
13	chr1:215729059..215730729-chr1:215736109..215738919,2	MCF-7	breast:
14	chr1:215726004..215728201-chr1:215739965..215741596,2	MCF-7	breast:
15	chr1:215722423..215725926-chr1:215740211..215742928,3	K562	blood:
16	chr1:215741634..215744285-chr1:215769987..215771958,3	K562	blood:
17	chr1:215727802..215730014-chr1:215737556..215740283,2	K562	blood:
18	chr1:215727863..215730220-chr1:215736025..215738063,2	K562	blood:
19	chr1:215727863..215730220-chr1:215736025..215738063,2	K562	blood:
20	chr1:215727846..215730896-chr1:215740314..215742858,4	K562	blood:
21	chr1:215728975..215731835-chr1:215739008..215743111,5	MCF-7	breast:
22	chr1:215740294..215741084-chr19:3985081..3985884,2	Hela-S3	cervix:
23	chr1:215655508..215656065-chr1:215718108..215718963,2	MCF-7	breast:
24	chr1:215740395..215741072-chr11:62608879..62609640,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USH2A-1	chr1:215740146-215740734	NONHSAT009473

No data

Variant related genes	Relation type
KCTD3	TF binding region
KCTD3	CpG island
ENSG00000167658	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000136636	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000111678	chromatin interactions

Extended variants
information (count: 863 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:863 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547650131	chr1:215717627-215717628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537777196	chr1:215717640-215717641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367815968	chr1:215717654-215717655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547756545	chr1:215717656-215717657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570628544	chr1:215717671-215717672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539737278	chr1:215717683-215717684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549667793	chr1:215717713-215717714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79762302	chr1:215717743-215717744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143971783	chr1:215717757-215717758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555479251	chr1:215717760-215717761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572092103	chr1:215717761-215717762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150911214	chr1:215717798-215717799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372971066	chr1:215717941-215717942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558153501	chr1:215717942-215717943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139387686	chr1:215717967-215717968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544100514	chr1:215717975-215717976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377527055	chr1:215717992-215717993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112554451	chr1:215718023-215718024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186926667	chr1:215718088-215718089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541931674	chr1:215718101-215718102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566232944	chr1:215718150-215718151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546307146	chr1:215718240-215718241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527407049	chr1:215718241-215718242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370388624	chr1:215718294-215718295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116614268	chr1:215718295-215718296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376442669	chr1:215718300-215718301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533030153	chr1:215718359-215718360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550093094	chr1:215718444-215718445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190120657	chr1:215718452-215718453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535297641	chr1:215718456-215718457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373334848	chr1:215718469-215718470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565807332	chr1:215718501-215718502	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs535134745	chr1:215718553-215718554	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs557825778	chr1:215718558-215718559	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs115191634	chr1:215718619-215718620	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs537335571	chr1:215718625-215718626	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs557670593	chr1:215718647-215718648	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs115693378	chr1:215718662-215718663	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs73083482	chr1:215718666-215718667	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs553622389	chr1:215718684-215718685	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs145375462	chr1:215718686-215718687	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs111361371	chr1:215718699-215718700	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560294760	chr1:215718725-215718726	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs538032539	chr1:215718747-215718748	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs73083483	chr1:215718766-215718767	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532982112	chr1:215718801-215718802	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs543333508	chr1:215718821-215718822	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs181179007	chr1:215718848-215718849	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529171709	chr1:215718865-215718866	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548732606	chr1:215718885-215718886	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215715000-215719600	Enhancers	Colon Smooth Muscle	Colon
2	chr1:215716600-215717800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr1:215717800-215718800	Enhancers	Rectal Smooth Muscle	rectum
4	chr1:215718800-215720200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr1:215719600-215721000	Weak transcription	Colon Smooth Muscle	Colon
6	chr1:215720200-215722000	Enhancers	Rectal Smooth Muscle	rectum
7	chr1:215720800-215721200	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr1:215721000-215721400	Enhancers	Colon Smooth Muscle	Colon
9	chr1:215728600-215730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:215729000-215730400	Weak transcription	Pancreas	Pancrea
11	chr1:215729600-215729800	Enhancers	Duodenum Mucosa	Duodenum
12	chr1:215729600-215731200	ZNF genes & repeats	Fetal Intestine Small	intestine
13	chr1:215729800-215730200	ZNF genes & repeats	Spleen	Spleen
14	chr1:215729800-215730600	Flanking Active TSS	Duodenum Mucosa	Duodenum
15	chr1:215729800-215730800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:215730000-215730200	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr1:215730000-215730600	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr1:215730000-215732000	Enhancers	Fetal Intestine Large	intestine
19	chr1:215730000-215732000	Enhancers	Stomach Mucosa	stomach
20	chr1:215730200-215730400	Active TSS	Spleen	Spleen
21	chr1:215730200-215730600	Enhancers	HepG2	liver
22	chr1:215730200-215731000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr1:215730400-215730600	Flanking Active TSS	Spleen	Spleen
24	chr1:215730400-215730800	Enhancers	Pancreas	Pancrea
25	chr1:215730400-215731000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr1:215730400-215732200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr1:215730600-215730800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:215730600-215732000	Flanking Active TSS	HepG2	liver
29	chr1:215730600-215732200	Enhancers	Duodenum Mucosa	Duodenum
30	chr1:215730800-215731800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr1:215730800-215732000	Enhancers	Liver	Liver
32	chr1:215730800-215740200	Weak transcription	Pancreas	Pancrea
33	chr1:215731000-215731800	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr1:215731200-215731600	Weak transcription	Fetal Intestine Small	intestine
35	chr1:215731800-215732000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr1:215731800-215732000	Enhancers	Fetal Intestine Small	intestine
37	chr1:215732000-215732800	Enhancers	HepG2	liver
38	chr1:215732000-215740200	Weak transcription	Stomach Mucosa	stomach
39	chr1:215732800-215734000	Weak transcription	HepG2	liver
40	chr1:215739000-215739200	Enhancers	Small Intestine	intestine
41	chr1:215739000-215739800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:215739000-215739800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:215739000-215739800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr1:215739000-215740000	Enhancers	Fetal Intestine Large	intestine
45	chr1:215739200-215739400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr1:215739200-215739400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:215739200-215739400	Enhancers	Brain Germinal Matrix	brain
48	chr1:215739200-215739400	Enhancers	Colon Smooth Muscle	Colon
49	chr1:215739200-215739800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr1:215739200-215739800	Enhancers	Duodenum Mucosa	Duodenum

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