Variant report

Variant	nsv521769
Chromosome Location	chr1:71578442-71633719
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:71602134-71602422	HepG2	liver:	n/a	chr1:71602303-71602314
2	CEBPB	chr1:71625376-71625509	A549	lung:	n/a	chr1:71625437-71625450 chr1:71625438-71625449
3	CEBPB	chr1:71625304-71625534	HepG2	liver:	n/a	chr1:71625437-71625450 chr1:71625438-71625449
4	CEBPB	chr1:71602123-71602413	IMR90	lung:	n/a	chr1:71602303-71602314
5	CEBPB	chr1:71602335-71602346	K562	blood:	n/a	n/a
6	CTCF	chr1:71584700-71584850	GM12878	blood:	n/a	n/a
7	CTCF	chr1:71582420-71582570	GM12872	blood:	n/a	n/a
8	CTCF	chr1:71612880-71613030	HEK293	kidney:	n/a	n/a
9	CTCF	chr1:71590311-71590344	Pancreas_OC	pancreas:	n/a	n/a
10	E2F4	chr1:71622896-71623128	MCF10A-Er-Src	breast:	n/a	n/a
11	EBF1	chr1:71626997-71627172	GM12878	blood:	n/a	n/a
12	FOS	chr1:71622914-71623114	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr1:71622905-71623108	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr1:71622904-71623107	MCF10A-Er-Src	breast:	n/a	n/a
15	FOXA1	chr1:71620232-71620432	ECC-1	luminal epithelium:	n/a	n/a
16	GATA3	chr1:71630400-71630551	SH-SY5Y	brain:	n/a	n/a
17	JUND	chr1:71632484-71632491	H1-hESC	embryonic stem cell:	n/a	n/a
18	KAP1	chr1:71591443-71591757	K562	blood:	n/a	n/a
19	KAP1	chr1:71622635-71623223	U2OS	brain:	n/a	n/a
20	KAP1	chr1:71600237-71600422	K562	blood:	n/a	n/a
21	MAFF	chr1:71613660-71614022	HepG2	liver:	n/a	chr1:71613828-71613846
22	MAFF	chr1:71613701-71613991	K562	blood:	n/a	chr1:71613828-71613846
23	MAFF	chr1:71578702-71578801	HepG2	liver:	n/a	n/a
24	MAFK	chr1:71613668-71614018	IMR90	lung:	n/a	chr1:71613830-71613845
25	MAFK	chr1:71578658-71578858	HepG2	liver:	n/a	n/a
26	MAFK	chr1:71630030-71630204	HepG2	liver:	n/a	n/a
27	MAFK	chr1:71613665-71614020	HepG2	liver:	n/a	chr1:71613830-71613845
28	MAFK	chr1:71613680-71614012	HepG2	liver:	n/a	chr1:71613830-71613845
29	MAFK	chr1:71613780-71613914	H1-hESC	embryonic stem cell:	n/a	chr1:71613830-71613845
30	MAFK	chr1:71613714-71613974	K562	blood:	n/a	chr1:71613830-71613845
31	MAFK	chr1:71613752-71614031	GM12878	blood:	n/a	chr1:71613830-71613845
32	MAFK	chr1:71613699-71613998	Hela-S3	cervix:	n/a	chr1:71613830-71613845
33	MAX	chr1:71582216-71582274	HepG2	liver:	n/a	n/a
34	MXI1	chr1:71625803-71625867	GM12878	blood:	n/a	n/a
35	MYC	chr1:71629642-71629712	H1-hESC	embryonic stem cell:	n/a	n/a
36	MYC	chr1:71614825-71614943	MCF10A-Er-Src	breast:	n/a	n/a
37	NFYB	chr1:71629503-71629703	GM12878	blood:	n/a	n/a
38	POLR2A	chr1:71621553-71621576	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr1:71625350-71625371	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr1:71593704-71594205	H1-neurons	neurons:	n/a	n/a
41	POLR2A	chr1:71623470-71623554	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr1:71624798-71624801	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr1:71593797-71594158	H1-neurons	neurons:	n/a	n/a
44	POLR2A	chr1:71595525-71595572	MCF-7	breast:	n/a	n/a
45	POLR2A	chr1:71578706-71578886	MCF10A-Er-Src	breast:	n/a	n/a
46	RFX5	chr1:71578765-71578853	K562	blood:	n/a	n/a
47	SPI1	chr1:71588528-71588880	GM12878	blood:	n/a	n/a
48	STAT3	chr1:71608176-71608376	MCF10A-Er-Src	breast:	n/a	n/a
49	STAT3	chr1:71606380-71606456	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr1:71629541-71629595	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71632244-71632294	AG04450	lung:	fetal
2	chr1:71632244-71632294	HMEC	breast:	n/a
3	chr1:71632244-71632294	MCF10A-Er-Src	breast:	n/a
4	chr1:71632244-71632294	AG09309	skin:	n/a
5	chr1:71632244-71632294	AoSMC	blood vessel:	n/a
6	chr1:71632244-71632294	NHDF-neo	bronchial:	n/a
7	chr1:71632244-71632294	MCF-7	breast:	n/a
8	chr1:71632244-71632294	NH-A	brain:	n/a
9	chr1:71632244-71632294	NHBE	bronchial:	n/a
10	chr1:71632244-71632294	K562	blood:	n/a
11	chr1:71632244-71632294	AG10803	skin:	n/a
12	chr1:71632244-71632294	HRE	kidney:	n/a
13	chr1:71632244-71632294	LNCaP	prostate:	n/a
14	chr1:71632244-71632294	HNPCEpiC	eye:	n/a
15	chr1:71632244-71632294	NB4	blood:	n/a
16	chr1:71632244-71632294	AG09319	gingival:	n/a
17	chr1:71632244-71632294	PANC-1	pancreas:	n/a
18	chr1:71632244-71632294	HCPEpiC	choroid plexus:	n/a
19	chr1:71632244-71632294	HUVEC	blood vessel:	n/a
20	chr1:71632244-71632294	ProgFib	skin:	n/a
21	chr1:71632244-71632294	CMK	blood:	n/a
22	chr1:71632244-71632294	HIPEpiC	eye:	n/a
23	chr1:71632244-71632294	PrEC	prostate:	n/a
24	chr1:71632244-71632294	H1-hESC	embryonic stem cell:	embryo
25	chr1:71632244-71632294	HAEpiC	amniotic membrane:	n/a
26	chr1:71632244-71632294	Caco-2	colon:	n/a
27	chr1:71632244-71632294	ovcar-3	ovarian:	n/a
28	chr1:71632244-71632294	HepG2	liver:	n/a
29	chr1:71632244-71632294	GM12878	blood:	n/a
30	chr1:71632244-71632294	HL-60	blood:	n/a
31	chr1:71632244-71632294	SK-N-SH_RA	brain:	n/a
32	chr1:71632244-71632294	GM12891	blood:	n/a
33	chr1:71632244-71632294	GM19239	blood:	n/a
34	chr1:71632244-71632294	SAEC	small airway:	n/a
35	chr1:71632244-71632294	GM06990	blood:	n/a
36	chr1:71632244-71632294	HCF	heart:	n/a
37	chr1:71632244-71632294	HEK293	kidney:	embryo
38	chr1:71632244-71632294	T-47D	breast:	n/a
39	chr1:71632244-71632294	Jurkat	blood:	n/a
40	chr1:71632244-71632294	HRCEpiC	kidney:	n/a
41	chr1:71632244-71632294	SKMC	muscle:	n/a
42	chr1:71632244-71632294	Hela-S3	cervix:	n/a
43	chr1:71632244-71632294	AG04449	skin:	fetal
44	chr1:71632244-71632294	U87	brain:	n/a
45	chr1:71632244-71632294	BE2_C	brain:	n/a
46	chr1:71632244-71632294	HRPEpiC	eye:	n/a
47	chr1:71632244-71632294	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:71632244-71632294	BJ	skin:	n/a
49	chr1:71632244-71632294	A549	lung:	n/a
50	chr1:71632244-71632294	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:71561763..71564195-chr1:71605230..71607303,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000264239	TF binding region
ENSG00000264239	CpG island

Extended variants
information (count: 736 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556495733	chr1:71582316-71582317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192393301	chr1:71582333-71582334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538821381	chr1:71582345-71582346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35135405	chr1:71582357-71582358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116583845	chr1:71582370-71582371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs578024748	chr1:71582375-71582376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540282465	chr1:71582386-71582387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554094510	chr1:71582396-71582397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138551823	chr1:71582414-71582415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114066034	chr1:71582421-71582422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562829316	chr1:71582454-71582455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74090289	chr1:71582470-71582471	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs367955699	chr1:71582479-71582480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528632370	chr1:71582491-71582492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545558721	chr1:71582501-71582502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539923200	chr1:71582506-71582507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148294621	chr1:71582507-71582508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373187699	chr1:71582523-71582524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573158333	chr1:71582532-71582533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74090292	chr1:71582534-71582535	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs547082395	chr1:71582552-71582553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370992365	chr1:71582633-71582634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547148255	chr1:71582692-71582693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567318657	chr1:71582715-71582716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529705304	chr1:71582843-71582844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144075938	chr1:71582891-71582892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184496523	chr1:71582944-71582945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189017057	chr1:71583017-71583018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538478315	chr1:71583075-71583076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540279581	chr1:71583093-71583094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181570724	chr1:71583130-71583131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370758830	chr1:71583159-71583160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115055331	chr1:71583160-71583161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34817044	chr1:71583168-71583169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534251105	chr1:71583172-71583173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147358914	chr1:71583181-71583182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573734937	chr1:71583228-71583229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184750040	chr1:71583281-71583282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139450244	chr1:71583332-71583333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374758003	chr1:71583357-71583358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544143806	chr1:71583411-71583412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556464788	chr1:71583513-71583514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576296471	chr1:71583535-71583536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545282635	chr1:71583612-71583613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565433682	chr1:71583628-71583629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs5775050	chr1:71583630-71583631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs36027042	chr1:71583631-71583632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs3048509	chr1:71583632-71583633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559731454	chr1:71583667-71583668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565911820	chr1:71584221-71584222	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71582200-71582600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:71582200-71582600	Enhancers	Fetal Brain Male	brain
3	chr1:71582200-71583800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr1:71582600-71583000	Weak transcription	Fetal Brain Male	brain
5	chr1:71583000-71583600	Enhancers	Fetal Brain Male	brain
6	chr1:71583400-71583600	Enhancers	HSMMtube	muscle
7	chr1:71584200-71584400	Enhancers	HSMMtube	muscle
8	chr1:71595400-71595800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:71595400-71595800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:71595400-71596800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
11	chr1:71595600-71595800	ZNF genes & repeats	Pancreas	Pancrea
12	chr1:71599600-71600400	ZNF genes & repeats	Liver	Liver
13	chr1:71618000-71623800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:71619600-71620600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:71619800-71624400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:71620200-71620400	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr1:71620200-71620600	Enhancers	Gastric	stomach
18	chr1:71620200-71622800	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr1:71620400-71621200	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr1:71620600-71620800	ZNF genes & repeats	Esophagus	oesophagus
21	chr1:71620600-71621000	Weak transcription	Gastric	stomach
22	chr1:71621000-71621400	Enhancers	Gastric	stomach
23	chr1:71621200-71621400	Enhancers	Lung	lung
24	chr1:71621200-71621800	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr1:71621200-71623600	Enhancers	Fetal Lung	lung
26	chr1:71621400-71621800	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr1:71621400-71622200	Enhancers	Colonic Mucosa	Colon
28	chr1:71621400-71623800	Weak transcription	Lung	lung
29	chr1:71621800-71623600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
30	chr1:71621800-71623800	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr1:71622000-71622800	Enhancers	Fetal Intestine Small	intestine
32	chr1:71622200-71622800	Weak transcription	Colonic Mucosa	Colon
33	chr1:71622400-71622800	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr1:71622800-71623000	Enhancers	Colonic Mucosa	Colon
35	chr1:71622800-71623200	Enhancers	Fetal Intestine Large	intestine
36	chr1:71622800-71623200	Weak transcription	Fetal Intestine Small	intestine
37	chr1:71622800-71623400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
38	chr1:71623200-71624000	Enhancers	Fetal Intestine Small	intestine
39	chr1:71623400-71623800	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr1:71623600-71624200	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr1:71623800-71624000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:71623800-71624000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
43	chr1:71623800-71624200	Enhancers	Lung	lung
44	chr1:71623800-71624200	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr1:71624000-71624400	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr1:71624200-71625200	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr1:71624400-71625000	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr1:71625200-71625400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr1:71625200-71625400	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr1:71625200-71625400	Enhancers	Sigmoid Colon	Sigmoid Colon

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