Variant report

Variant	esv1836983
Chromosome Location	chr7:100630638-100669857
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:822)
CpG islands
(count:855)
Chromatin interactive
region (count:14)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:822 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:100661797-100662462	GM12878	blood:	n/a	n/a
2	ATF2	chr7:100660727-100661099	GM12878	blood:	n/a	n/a
3	ATF2	chr7:100660670-100661107	GM12878	blood:	n/a	n/a
4	ATF3	chr7:100660850-100661016	K562	blood:	n/a	n/a
5	ATF3	chr7:100660660-100661103	A549	lung:	n/a	n/a
6	ATF3	chr7:100660675-100661110	A549	lung:	n/a	n/a
7	ATF3	chr7:100660800-100661128	K562	blood:	n/a	n/a
8	BACH1	chr7:100660799-100660996	K562	blood:	n/a	n/a
9	BACH1	chr7:100660771-100661027	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:100661967-100662417	GM12878	blood:	n/a	n/a
11	BATF	chr7:100662051-100662382	GM12878	blood:	n/a	n/a
12	BATF	chr7:100639506-100639706	GM12878	blood:	n/a	n/a
13	BATF	chr7:100642903-100643274	GM12878	blood:	n/a	n/a
14	BATF	chr7:100660816-100661103	GM12878	blood:	n/a	n/a
15	BATF	chr7:100638232-100638603	GM12878	blood:	n/a	n/a
16	BATF	chr7:100639500-100639767	GM12878	blood:	n/a	n/a
17	BATF	chr7:100660711-100661146	GM12878	blood:	n/a	n/a
18	BATF	chr7:100644177-100644377	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:100636871-100637170	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:100641497-100641810	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:100642244-100642522	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:100642996-100643389	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:100638325-100638704	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:100643073-100643393	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:100644120-100644394	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:100644746-100645059	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:100640075-100640388	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:100636278-100636436	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:100635815-100636015	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:100643645-100643874	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:100661969-100662354	GM12878	blood:	n/a	chr7:100662223-100662232
32	BCL11A	chr7:100660767-100661112	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:100640822-100641084	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:100639449-100639723	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:100638402-100638714	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:100637602-100637835	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:100660848-100661165	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:100645493-100645916	GM12878	blood:	n/a	n/a
39	BCL3	chr7:100660552-100661086	A549	lung:	n/a	n/a
40	BCL3	chr7:100660686-100661198	GM12878	blood:	n/a	n/a
41	BCL3	chr7:100660242-100661162	A549	lung:	n/a	n/a
42	BCLAF1	chr7:100661927-100662319	GM12878	blood:	n/a	chr7:100662223-100662232
43	BHLHE40	chr7:100660843-100660996	HepG2	liver:	n/a	n/a
44	BHLHE40	chr7:100660484-100661125	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:100660870-100660995	K562	blood:	n/a	n/a
46	BHLHE40	chr7:100660487-100660610	K562	blood:	n/a	n/a
47	BHLHE40	chr7:100661909-100662190	GM12878	blood:	n/a	n/a
48	BRCA1	chr7:100660746-100660924	HepG2	liver:	n/a	n/a
49	CBX3	chr7:100660230-100661139	K562	blood:	n/a	n/a
50	CCNT2	chr7:100660408-100660966	K562	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100663239-100663289	SK-N-MC	brain:	n/a
2	chr7:100663239-100663289	SK-N-MC	brain:	n/a
3	chr7:100663367-100663417	Hepatocyte	liver:	n/a
4	chr7:100647879-100647929	HRE	kidney:	n/a
5	chr7:100661991-100662041	ovcar-3	ovarian:	n/a
6	chr7:100660494-100660544	K562	blood:	n/a
7	chr7:100662570-100662620	HepG2	liver:	n/a
8	chr7:100647829-100647879	HRPEpiC	eye:	n/a
9	chr7:100662570-100662620	HIPEpiC	eye:	n/a
10	chr7:100647879-100647929	MCF-7	breast:	n/a
11	chr7:100660909-100660959	NH-A	brain:	n/a
12	chr7:100646795-100646845	MCF-7	breast:	n/a
13	chr7:100663239-100663289	HCT-116	colon:	n/a
14	chr7:100663239-100663289	RPTEC	kidney:	n/a
15	chr7:100636153-100636203	HRE	kidney:	n/a
16	chr7:100647879-100647929	SAEC	small airway:	n/a
17	chr7:100663239-100663289	NT2-D1	testis:	n/a
18	chr7:100663239-100663289	HCM	heart:	n/a
19	chr7:100647879-100647929	AG09319	gingival:	n/a
20	chr7:100661996-100662046	HUVEC	blood vessel:	n/a
21	chr7:100663239-100663289	HEEpiC	esophagus:	n/a
22	chr7:100661996-100662046	T-47D	breast:	n/a
23	chr7:100646795-100646845	MCF10A-Er-Src	breast:	n/a
24	chr7:100636153-100636203	PANC-1	pancreas:	n/a
25	chr7:100660909-100660959	BJ	skin:	n/a
26	chr7:100660494-100660544	PFSK-1	brain:	n/a
27	chr7:100646795-100646845	Hepatocyte	liver:	n/a
28	chr7:100660494-100660544	Jurkat	blood:	n/a
29	chr7:100636153-100636203	HEK293	kidney:	embryo
30	chr7:100660595-100660645	Caco-2	colon:	n/a
31	chr7:100660494-100660544	AG04449	skin:	fetal
32	chr7:100660595-100660645	ECC-1	luminal epithelium:	n/a
33	chr7:100660909-100660959	A549	lung:	n/a
34	chr7:100661996-100662046	HCM	heart:	n/a
35	chr7:100660595-100660645	HCPEpiC	choroid plexus:	n/a
36	chr7:100663239-100663289	MCF-7	breast:	n/a
37	chr7:100636153-100636203	HL-60	blood:	n/a
38	chr7:100661996-100662046	GM06990	blood:	n/a
39	chr7:100660909-100660959	AG04449	skin:	fetal
40	chr7:100647829-100647879	GM12878	blood:	n/a
41	chr7:100661996-100662046	ovcar-3	ovarian:	n/a
42	chr7:100663367-100663417	HL-60	blood:	n/a
43	chr7:100663185-100663235	HPAEpiC	pulmonary alveolar:	n/a
44	chr7:100646795-100646845	HUVEC	blood vessel:	n/a
45	chr7:100646795-100646845	HCPEpiC	choroid plexus:	n/a
46	chr7:100660909-100660959	ovcar-3	ovarian:	n/a
47	chr7:100663239-100663289	NHBE	bronchial:	n/a
48	chr7:100661991-100662041	IMR90	lung:	fetal
49	chr7:100647879-100647929	AG04450	lung:	fetal
50	chr7:100646795-100646845	CMK	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100606234..100609871-chr7:100659072..100662376,5	K562	blood:
2	chr7:100648211..100651401-chr7:100653251..100655813,3	K562	blood:
3	chr7:100648084..100649778-chr7:100660214..100661843,2	MCF-7	breast:
4	chr7:100663659..100665527-chr7:100686154..100687748,2	K562	blood:
5	chr7:100462781..100465423-chr7:100657982..100660007,2	MCF-7	breast:
6	chr7:100608767..100609716-chr7:100660411..100661061,2	K562	blood:
7	chr7:100661599..100663275-chr7:100811718..100814144,2	K562	blood:
8	chr7:100648211..100651401-chr7:100653251..100655813,3	K562	blood:
9	chr7:100650929..100652882-chr7:100660987..100663735,2	K562	blood:
10	chr7:100651695..100653589-chr7:100673839..100675756,2	MCF-7	breast:
11	chr7:100609382..100610920-chr7:100667758..100669806,2	MCF-7	breast:
12	chr7:100486083..100488238-chr7:100659648..100662388,2	MCF-7	breast:
13	chr7:100651588..100653304-chr7:100658746..100661448,2	K562	blood:
14	chr7:100486496..100489438-chr7:100663883..100665866,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACHE-6	chr7:100647545-100647615	NONHSAT122434
2	lnc-VGF-1	chr7:100657601-100657720	ENSG00000227053.1
3	lnc-VGF-1	chr7:100660696-100660882	ENSG00000227053.1
4	lnc-MUC17-1	chr7:100661876-100662220	NONHSAT122439
5	lnc-MUC17-1	chr7:100660856-100660944	NONHSAT122438
6	lnc-MUC17-1	chr7:100661876-100662217	NONHSAT122438
7	lnc-VGF-1	chr7:100658479-100658548	ENSG00000227053.1
8	lnc-VGF-1	chr7:100658479-100658571	ENSG00000227053.1
9	lnc-MUC17-1	chr7:100660544-100660678	NONHSAT122438
10	lnc-MUC17-1	chr7:100660615-100660944	NONHSAT122439
11	lnc-ACHE-6	chr7:100643354-100643800	NONHSAT122434
12	lnc-VGF-1	chr7:100657606-100657720	ENSG00000227053.1
13	lnc-VGF-1	chr7:100660696-100660889	ENSG00000227053.1
14	lnc-VGF-2	chr7:100665373-100665608	expReg_chr7_6684_-

No data

Variant related genes	Relation type
ENSG00000227053	TF binding region
MUC17	TF binding region
MUC12	TF binding region
ENSG00000227053	CpG island
MUC17	CpG island
MUC12	CpG island
ENSG00000087077	chromatin interactions
ENSG00000176125	chromatin interactions
ENSG00000169876	chromatin interactions
ENSG00000169894	chromatin interactions
ENSG00000227053	chromatin interactions
ENSG00000225946	chromatin interactions
ENSG00000205277	chromatin interactions

Extended variants
information (count: 1864 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1864 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573825961	chr7:100630657-100630658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371002892	chr7:100630658-100630659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531070523	chr7:100630680-100630681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552381757	chr7:100630704-100630705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570559605	chr7:100630728-100630729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs58231202	chr7:100630739-100630740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186426231	chr7:100630756-100630757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561938795	chr7:100630816-100630817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56036334	chr7:100630828-100630829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547298903	chr7:100630834-100630835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541836863	chr7:100630842-100630843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565603033	chr7:100630878-100630879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142484321	chr7:100630932-100630933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554775417	chr7:100630979-100630980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7457468	chr7:100630990-100630991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs189950733	chr7:100631029-100631030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35019357	chr7:100631143-100631144	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs576907718	chr7:100631148-100631149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144516841	chr7:100631176-100631177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564417088	chr7:100631208-100631209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs6963607	chr7:100631233-100631234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs3891963	chr7:100631247-100631248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs34064326	chr7:100631251-100631252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112698224	chr7:100631252-100631253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375756695	chr7:100631267-100631268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187223430	chr7:100631299-100631300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs36035785	chr7:100631307-100631308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190122442	chr7:100631338-100631339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545897612	chr7:100631342-100631343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368136528	chr7:100631354-100631355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372155609	chr7:100631435-100631436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552595829	chr7:100631436-100631437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528482509	chr7:100631445-100631446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546561763	chr7:100631450-100631451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561725001	chr7:100631482-100631483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530036221	chr7:100631508-100631509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529568665	chr7:100631533-100631534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569877720	chr7:100631561-100631562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78552568	chr7:100631570-100631571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35427068	chr7:100631571-100631572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553892059	chr7:100631572-100631573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183483736	chr7:100631573-100631574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79876820	chr7:100631589-100631590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs202132480	chr7:100631593-100631594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552309123	chr7:100631674-100631675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112360007	chr7:100631717-100631718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371865272	chr7:100631734-100631735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116766914	chr7:100631748-100631749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534687327	chr7:100631784-100631785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553042277	chr7:100631807-100631808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100625000-100633400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr7:100625000-100634800	Weak transcription	Spleen	Spleen
3	chr7:100625600-100635000	Weak transcription	Right Atrium	heart
4	chr7:100627400-100632000	Weak transcription	Fetal Intestine Small	intestine
5	chr7:100627600-100633400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:100627600-100634200	Weak transcription	Colonic Mucosa	Colon
7	chr7:100630600-100630800	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr7:100630800-100633200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr7:100633200-100637800	Strong transcription	Rectal Mucosa Donor 31	rectum
10	chr7:100633400-100635400	Strong transcription	Rectal Mucosa Donor 29	rectum
11	chr7:100633400-100636400	Strong transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:100634200-100635000	Weak transcription	Rectal Smooth Muscle	rectum
13	chr7:100634200-100635600	Strong transcription	Colonic Mucosa	Colon
14	chr7:100634800-100635800	ZNF genes & repeats	Spleen	Spleen
15	chr7:100635000-100635200	Bivalent Enhancer	Fetal Stomach	stomach
16	chr7:100635000-100635400	ZNF genes & repeats	Gastric	stomach
17	chr7:100635000-100635800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:100635000-100635800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
19	chr7:100635000-100635800	ZNF genes & repeats	Right Atrium	heart
20	chr7:100635400-100635800	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
21	chr7:100635400-100660000	Weak transcription	Gastric	stomach
22	chr7:100635600-100635800	Enhancers	Fetal Muscle Trunk	muscle
23	chr7:100635600-100648200	Weak transcription	Colonic Mucosa	Colon
24	chr7:100635800-100636400	Strong transcription	Rectal Mucosa Donor 29	rectum
25	chr7:100635800-100660000	Weak transcription	Rectal Smooth Muscle	rectum
26	chr7:100635800-100660200	Weak transcription	Right Atrium	heart
27	chr7:100636400-100642600	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr7:100636400-100647800	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr7:100637800-100641800	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr7:100641800-100644000	Strong transcription	Rectal Mucosa Donor 31	rectum
31	chr7:100642400-100643000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr7:100642600-100643600	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr7:100642800-100643400	Weak transcription	Fetal Intestine Small	intestine
34	chr7:100643200-100643600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr7:100643200-100643600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr7:100643200-100643600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:100643400-100643600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr7:100643400-100643800	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr7:100643600-100647800	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr7:100643800-100655400	Weak transcription	Fetal Intestine Small	intestine
41	chr7:100644000-100647800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr7:100647800-100650000	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr7:100647800-100659000	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr7:100647800-100660200	Strong transcription	Rectal Mucosa Donor 31	rectum
45	chr7:100648200-100648400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr7:100648200-100648800	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr7:100648200-100648800	Strong transcription	Colonic Mucosa	Colon
48	chr7:100648400-100648600	Enhancers	Spleen	Spleen
49	chr7:100648800-100651600	Weak transcription	Colonic Mucosa	Colon
50	chr7:100648800-100659000	Weak transcription	Spleen	Spleen

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