Variant report

Variant	nsv820330
Chromosome Location	chr7:100630947-100656356
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:431)
CpG islands
(count:245)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:100639506-100639706	GM12878	blood:	n/a	n/a
2	BATF	chr7:100642903-100643274	GM12878	blood:	n/a	n/a
3	BATF	chr7:100644177-100644377	GM12878	blood:	n/a	n/a
4	BATF	chr7:100638232-100638603	GM12878	blood:	n/a	n/a
5	BATF	chr7:100639500-100639767	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:100643645-100643874	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:100635815-100636015	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:100639449-100639723	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:100645493-100645916	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:100637602-100637835	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:100644746-100645059	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:100642244-100642522	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:100641497-100641810	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:100638402-100638714	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:100643073-100643393	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:100636871-100637170	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:100644120-100644394	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:100640822-100641084	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:100638325-100638704	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:100636278-100636436	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:100640075-100640388	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:100642996-100643389	GM12878	blood:	n/a	n/a
23	CEBPB	chr7:100653277-100653286	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr7:100653204-100653373	K562	blood:	n/a	chr7:100653275-100653288
25	CTCF	chr7:100637488-100637533	LNCaP	prostate:	n/a	n/a
26	CTCF	chr7:100646660-100646857	K562	blood:	n/a	n/a
27	CTCF	chr7:100643321-100643608	K562	blood:	n/a	n/a
28	CTCF	chr7:100638295-100638342	LNCaP	prostate:	n/a	n/a
29	CTCF	chr7:100652620-100652770	A549	lung:	n/a	n/a
30	CTCF	chr7:100655522-100655567	LNCaP	prostate:	n/a	n/a
31	CTCF	chr7:100635640-100635790	GM12870	blood:	n/a	n/a
32	CTCF	chr7:100638850-100638927	LNCaP	prostate:	n/a	n/a
33	CTCF	chr7:100638800-100638950	K562	blood:	n/a	n/a
34	CTCF	chr7:100643442-100643617	LNCaP	prostate:	n/a	n/a
35	CTCF	chr7:100648440-100648590	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr7:100635659-100635788	HepG2	liver:	n/a	n/a
37	CTCF	chr7:100636726-100636745	LNCaP	prostate:	n/a	n/a
38	CTCF	chr7:100638800-100638950	HepG2	liver:	n/a	n/a
39	CTCF	chr7:100635680-100635830	K562	blood:	n/a	n/a
40	CTCF	chr7:100641906-100641942	LNCaP	prostate:	n/a	n/a
41	CTCF	chr7:100639506-100639602	LNCaP	prostate:	n/a	n/a
42	CTCF	chr7:100640050-100640068	LNCaP	prostate:	n/a	n/a
43	CTCF	chr7:100643540-100643690	AG09309	skin:	n/a	n/a
44	CTCF	chr7:100646576-100646659	LNCaP	prostate:	n/a	n/a
45	CTCF	chr7:100655481-100655577	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:100655501-100655581	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:100642179-100642204	LNCaP	prostate:	n/a	n/a
48	CTCF	chr7:100652460-100652610	Caco-2	colon:	n/a	n/a
49	CTCF	chr7:100655480-100655630	A549	lung:	n/a	n/a
50	CTCF	chr7:100642480-100642630	AoAF	blood vessel:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100647829-100647879	RPTEC	kidney:	n/a
2	chr7:100647829-100647879	RPTEC	kidney:	n/a
3	chr7:100647829-100647879	NHDF-neo	bronchial:	n/a
4	chr7:100647879-100647929	NB4	blood:	n/a
5	chr7:100646795-100646845	GM12878	blood:	n/a
6	chr7:100647829-100647879	HCM	heart:	n/a
7	chr7:100646795-100646845	H1-hESC	embryonic stem cell:	embryo
8	chr7:100647879-100647929	HEK293	kidney:	embryo
9	chr7:100647829-100647879	NHBE	bronchial:	n/a
10	chr7:100636153-100636203	HL-60	blood:	n/a
11	chr7:100636153-100636203	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:100636153-100636203	RPTEC	kidney:	n/a
13	chr7:100647879-100647929	HAEpiC	amniotic membrane:	n/a
14	chr7:100636153-100636203	NH-A	brain:	n/a
15	chr7:100636153-100636203	A549	lung:	n/a
16	chr7:100646795-100646845	Hepatocyte	liver:	n/a
17	chr7:100646795-100646845	HIPEpiC	eye:	n/a
18	chr7:100636153-100636203	BE2_C	brain:	n/a
19	chr7:100636153-100636203	AG09319	gingival:	n/a
20	chr7:100636153-100636203	HCF	heart:	n/a
21	chr7:100647879-100647929	HNPCEpiC	eye:	n/a
22	chr7:100647829-100647879	Caco-2	colon:	n/a
23	chr7:100636153-100636203	GM19239	blood:	n/a
24	chr7:100647879-100647929	IMR90	lung:	fetal
25	chr7:100647879-100647929	HRE	kidney:	n/a
26	chr7:100646795-100646845	HepG2	liver:	n/a
27	chr7:100647879-100647929	HCM	heart:	n/a
28	chr7:100646795-100646845	HCPEpiC	choroid plexus:	n/a
29	chr7:100647829-100647879	SK-N-MC	brain:	n/a
30	chr7:100636153-100636203	HUVEC	blood vessel:	n/a
31	chr7:100647879-100647929	GM19239	blood:	n/a
32	chr7:100646795-100646845	GM19239	blood:	n/a
33	chr7:100636153-100636203	SK-N-MC	brain:	n/a
34	chr7:100647829-100647879	GM12891	blood:	n/a
35	chr7:100647829-100647879	SKMC	muscle:	n/a
36	chr7:100647829-100647879	AG04449	skin:	fetal
37	chr7:100647879-100647929	ECC-1	luminal epithelium:	n/a
38	chr7:100646795-100646845	NHDF-neo	bronchial:	n/a
39	chr7:100647879-100647929	ovcar-3	ovarian:	n/a
40	chr7:100646795-100646845	IMR90	lung:	fetal
41	chr7:100647879-100647929	HRCEpiC	kidney:	n/a
42	chr7:100646795-100646845	GM06990	blood:	n/a
43	chr7:100646795-100646845	ProgFib	skin:	n/a
44	chr7:100647879-100647929	HCPEpiC	choroid plexus:	n/a
45	chr7:100636153-100636203	GM12892	blood:	n/a
46	chr7:100636153-100636203	GM12891	blood:	n/a
47	chr7:100647879-100647929	HCF	heart:	n/a
48	chr7:100647879-100647929	Hela-S3	cervix:	n/a
49	chr7:100636153-100636203	H1-hESC	embryonic stem cell:	embryo
50	chr7:100636153-100636203	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:100650929..100652882-chr7:100660987..100663735,2	K562	blood:
2	chr7:100651588..100653304-chr7:100658746..100661448,2	K562	blood:
3	chr7:100648211..100651401-chr7:100653251..100655813,3	K562	blood:
4	chr7:100648211..100651401-chr7:100653251..100655813,3	K562	blood:
5	chr7:100648084..100649778-chr7:100660214..100661843,2	MCF-7	breast:
6	chr7:100651695..100653589-chr7:100673839..100675756,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACHE-6	chr7:100643354-100643800	NONHSAT122434
2	lnc-ACHE-6	chr7:100647545-100647615	NONHSAT122434

No data

Variant related genes	Relation type
MUC12	TF binding region
MUC12	CpG island
ENSG00000205277	chromatin interactions
ENSG00000227053	chromatin interactions
ENSG00000169876	chromatin interactions

Extended variants
information (count: 1295 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1295 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554775417	chr7:100630979-100630980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7457468	chr7:100630990-100630991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs189950733	chr7:100631029-100631030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35019357	chr7:100631143-100631144	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs576907718	chr7:100631148-100631149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144516841	chr7:100631176-100631177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564417088	chr7:100631208-100631209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6963607	chr7:100631233-100631234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs3891963	chr7:100631247-100631248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs34064326	chr7:100631251-100631252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112698224	chr7:100631252-100631253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375756695	chr7:100631267-100631268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187223430	chr7:100631299-100631300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs36035785	chr7:100631307-100631308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190122442	chr7:100631338-100631339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545897612	chr7:100631342-100631343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368136528	chr7:100631354-100631355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372155609	chr7:100631435-100631436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552595829	chr7:100631436-100631437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528482509	chr7:100631445-100631446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546561763	chr7:100631450-100631451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561725001	chr7:100631482-100631483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530036221	chr7:100631508-100631509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529568665	chr7:100631533-100631534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569877720	chr7:100631561-100631562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78552568	chr7:100631570-100631571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35427068	chr7:100631571-100631572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553892059	chr7:100631572-100631573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183483736	chr7:100631573-100631574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79876820	chr7:100631589-100631590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs202132480	chr7:100631593-100631594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552309123	chr7:100631674-100631675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112360007	chr7:100631717-100631718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371865272	chr7:100631734-100631735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116766914	chr7:100631748-100631749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534687327	chr7:100631784-100631785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553042277	chr7:100631807-100631808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192900508	chr7:100631845-100631846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539430768	chr7:100631859-100631860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77326780	chr7:100631863-100631864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557325501	chr7:100631865-100631866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575806367	chr7:100631889-100631890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185807535	chr7:100631921-100631922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375269537	chr7:100631974-100631975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187706398	chr7:100632015-100632016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540314333	chr7:100632048-100632049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557922644	chr7:100632114-100632115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146988171	chr7:100632122-100632123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138368031	chr7:100632123-100632124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569630040	chr7:100632135-100632136	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:106 , 50 per page) page: 1 2 3

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	chr7:100630800-100633200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr7:100633200-100637800	Strong transcription	Rectal Mucosa Donor 31	rectum
9	chr7:100633400-100635400	Strong transcription	Rectal Mucosa Donor 29	rectum
10	chr7:100633400-100636400	Strong transcription	Sigmoid Colon	Sigmoid Colon
11	chr7:100634200-100635000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr7:100634200-100635600	Strong transcription	Colonic Mucosa	Colon
13	chr7:100634800-100635800	ZNF genes & repeats	Spleen	Spleen
14	chr7:100635000-100635200	Bivalent Enhancer	Fetal Stomach	stomach
15	chr7:100635000-100635400	ZNF genes & repeats	Gastric	stomach
16	chr7:100635000-100635800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:100635000-100635800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
18	chr7:100635000-100635800	ZNF genes & repeats	Right Atrium	heart
19	chr7:100635400-100635800	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
20	chr7:100635400-100660000	Weak transcription	Gastric	stomach
21	chr7:100635600-100635800	Enhancers	Fetal Muscle Trunk	muscle
22	chr7:100635600-100648200	Weak transcription	Colonic Mucosa	Colon
23	chr7:100635800-100636400	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr7:100635800-100660000	Weak transcription	Rectal Smooth Muscle	rectum
25	chr7:100635800-100660200	Weak transcription	Right Atrium	heart
26	chr7:100636400-100642600	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr7:100636400-100647800	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr7:100637800-100641800	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr7:100641800-100644000	Strong transcription	Rectal Mucosa Donor 31	rectum
30	chr7:100642400-100643000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:100642600-100643600	Strong transcription	Sigmoid Colon	Sigmoid Colon
32	chr7:100642800-100643400	Weak transcription	Fetal Intestine Small	intestine
33	chr7:100643200-100643600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr7:100643200-100643600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr7:100643200-100643600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:100643400-100643600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:100643400-100643800	ZNF genes & repeats	Fetal Intestine Small	intestine
38	chr7:100643600-100647800	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr7:100643800-100655400	Weak transcription	Fetal Intestine Small	intestine
40	chr7:100644000-100647800	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr7:100647800-100650000	Strong transcription	Sigmoid Colon	Sigmoid Colon
42	chr7:100647800-100659000	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr7:100647800-100660200	Strong transcription	Rectal Mucosa Donor 31	rectum
44	chr7:100648200-100648400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr7:100648200-100648800	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr7:100648200-100648800	Strong transcription	Colonic Mucosa	Colon
47	chr7:100648400-100648600	Enhancers	Spleen	Spleen
48	chr7:100648800-100651600	Weak transcription	Colonic Mucosa	Colon
49	chr7:100648800-100659000	Weak transcription	Spleen	Spleen
50	chr7:100649800-100650000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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