Variant report

Variant	nsv469562
Chromosome Location	chr4:70116673-70275787
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:736)
CpG islands
(count:62)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70254846-70255212	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70210667-70210694	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70274315-70274516	HepG2	liver:	n/a	n/a
4	ATF1	chr4:70175307-70175700	K562	blood:	n/a	n/a
5	ATF1	chr4:70187845-70188142	K562	blood:	n/a	n/a
6	BHLHE40	chr4:70209675-70209715	K562	blood:	n/a	n/a
7	CBX3	chr4:70175213-70175493	K562	blood:	n/a	n/a
8	CEBPB	chr4:70148592-70148690	A549	lung:	n/a	chr4:70148623-70148634
9	CEBPB	chr4:70148603-70148719	H1-hESC	embryonic stem cell:	n/a	chr4:70148623-70148634
10	CEBPB	chr4:70118972-70119263	HepG2	liver:	n/a	chr4:70119163-70119176
11	CEBPB	chr4:70254941-70255152	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:70221057-70221267	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:70148545-70148642	K562	blood:	n/a	chr4:70148623-70148634
14	CEBPB	chr4:70211562-70211766	HepG2	liver:	n/a	chr4:70211703-70211714
15	CEBPB	chr4:70226229-70226403	HepG2	liver:	n/a	chr4:70226280-70226289 chr4:70226280-70226291
16	CEBPB	chr4:70209480-70209728	K562	blood:	n/a	n/a
17	CTCF	chr4:70201320-70201470	GM12872	blood:	n/a	n/a
18	CTCF	chr4:70183686-70183869	MCF-7	breast:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
19	CTCF	chr4:70243460-70243610	MCF-7	breast:	n/a	n/a
20	CTCF	chr4:70183800-70183950	MCF-7	breast:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
21	CTCF	chr4:70201320-70201470	GM12874	blood:	n/a	n/a
22	CTCF	chr4:70183642-70183947	GM12878	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
23	CTCF	chr4:70183680-70183830	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr4:70201300-70201450	HPF	lung:	n/a	n/a
25	CTCF	chr4:70183706-70183971	A549	lung:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
26	CTCF	chr4:70201360-70201510	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr4:70183680-70183830	SAEC	small airway:	n/a	n/a
28	CTCF	chr4:70183800-70183950	NB4	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
29	CTCF	chr4:70201322-70201505	Gliobla	brain:	n/a	n/a
30	CTCF	chr4:70134405-70134621	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:70183720-70183870	AG09319	gingival:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
32	CTCF	chr4:70183629-70183965	K562	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
33	CTCF	chr4:70189120-70189270	HMF	breast:	n/a	n/a
34	CTCF	chr4:70183700-70183850	HBMEC	blood vessel:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
35	CTCF	chr4:70183720-70183870	NHLF	lung:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
36	CTCF	chr4:70183620-70183770	RPTEC	kidney:	n/a	n/a
37	CTCF	chr4:70183720-70183870	GM12873	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
38	CTCF	chr4:70175507-70175576	GM10266	blood:	n/a	n/a
39	CTCF	chr4:70142493-70142566	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr4:70201335-70201473	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr4:70201340-70201490	HPF	lung:	n/a	n/a
42	CTCF	chr4:70243427-70243527	A549	lung:	n/a	n/a
43	CTCF	chr4:70183680-70183830	GM12871	blood:	n/a	n/a
44	CTCF	chr4:70189180-70189330	K562	blood:	n/a	n/a
45	CTCF	chr4:70183720-70183870	NHEK	skin:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
46	CTCF	chr4:70201422-70201428	ProgFib	skin:	n/a	n/a
47	CTCF	chr4:70183739-70183847	MCF-7	breast:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
48	CTCF	chr4:70183660-70183810	HCM	heart:	n/a	n/a
49	CTCF	chr4:70201300-70201450	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr4:70183740-70183890	HMF	breast:	n/a	chr4:70183815-70183833 chr4:70183817-70183838

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70155747-70155797	HNPCEpiC	eye:	n/a
2	chr4:70155747-70155797	HNPCEpiC	eye:	n/a
3	chr4:70155747-70155797	NB4	blood:	n/a
4	chr4:70155747-70155797	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:70155747-70155797	GM19239	blood:	n/a
6	chr4:70155747-70155797	ECC-1	luminal epithelium:	n/a
7	chr4:70155747-70155797	AG04449	skin:	fetal
8	chr4:70155747-70155797	NT2-D1	testis:	n/a
9	chr4:70155747-70155797	RPTEC	kidney:	n/a
10	chr4:70155747-70155797	SK-N-SH	brain:	n/a
11	chr4:70155747-70155797	HepG2	liver:	n/a
12	chr4:70155747-70155797	Hepatocyte	liver:	n/a
13	chr4:70155747-70155797	A549	lung:	n/a
14	chr4:70155747-70155797	HCPEpiC	choroid plexus:	n/a
15	chr4:70155747-70155797	GM12878	blood:	n/a
16	chr4:70155747-70155797	SKMC	muscle:	n/a
17	chr4:70155747-70155797	K562	blood:	n/a
18	chr4:70155747-70155797	HIPEpiC	eye:	n/a
19	chr4:70155747-70155797	HAEpiC	amniotic membrane:	n/a
20	chr4:70155747-70155797	NHBE	bronchial:	n/a
21	chr4:70155747-70155797	HRE	kidney:	n/a
22	chr4:70155747-70155797	PANC-1	pancreas:	n/a
23	chr4:70155747-70155797	NH-A	brain:	n/a
24	chr4:70155747-70155797	HCM	heart:	n/a
25	chr4:70155747-70155797	HCT-116	colon:	n/a
26	chr4:70155747-70155797	AG10803	skin:	n/a
27	chr4:70155747-70155797	SK-N-MC	brain:	n/a
28	chr4:70155747-70155797	CMK	blood:	n/a
29	chr4:70155747-70155797	Caco-2	colon:	n/a
30	chr4:70155747-70155797	BE2_C	brain:	n/a
31	chr4:70155747-70155797	AoSMC	blood vessel:	n/a
32	chr4:70155747-70155797	MCF10A-Er-Src	breast:	n/a
33	chr4:70155747-70155797	MCF-7	breast:	n/a
34	chr4:70155747-70155797	HL-60	blood:	n/a
35	chr4:70155747-70155797	HRPEpiC	eye:	n/a
36	chr4:70155747-70155797	LNCaP	prostate:	n/a
37	chr4:70155747-70155797	GM12892	blood:	n/a
38	chr4:70155747-70155797	HCF	heart:	n/a
39	chr4:70155747-70155797	GM12891	blood:	n/a
40	chr4:70155747-70155797	NHDF-neo	bronchial:	n/a
41	chr4:70155747-70155797	Hela-S3	cervix:	n/a
42	chr4:70155747-70155797	SAEC	small airway:	n/a
43	chr4:70155747-70155797	ProgFib	skin:	n/a
44	chr4:70155747-70155797	U87	brain:	n/a
45	chr4:70155747-70155797	BJ	skin:	n/a
46	chr4:70155747-70155797	PFSK-1	brain:	n/a
47	chr4:70155747-70155797	HUVEC	blood vessel:	n/a
48	chr4:70155747-70155797	ovcar-3	ovarian:	n/a
49	chr4:70155747-70155797	AG09309	skin:	n/a
50	chr4:70155747-70155797	PrEC	prostate:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:45932378..45933054-chr4:70163468..70164237,2	MCF-7	breast:
2	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
3	chr4:70183340..70184245-chr4:70482427..70483057,3	MCF-7	breast:
4	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
5	chr4:70183605..70184238-chr4:70482598..70483352,3	MCF-7	breast:
6	chr4:69789542..69791043-chr4:70152702..70154403,2	MCF-7	breast:
7	chr4:70262708..70264895-chr4:70280098..70283006,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-4	chr4:70253298-70254025	NONHSAT096763
2	lnc-UGT2B28-5	chr4:70272649-70273373	NONHSAT096764

No data

Variant related genes	Relation type
ENSG00000251691	TF binding region
ENSG00000248824	TF binding region
ENSG00000268209	TF binding region
ENSG00000215110	TF binding region
ENSG00000249956	TF binding region
ENSG00000250612	TF binding region
UGT2B28	TF binding region
ENSG00000251691	CpG island
ENSG00000248824	CpG island
ENSG00000268209	CpG island
ENSG00000215110	CpG island
ENSG00000249956	CpG island
ENSG00000250612	CpG island
UGT2B28	CpG island
ENSG00000198277	chromatin interactions

Extended variants
information (count: 1645 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1645 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553840019	chr4:70132412-70132413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576932771	chr4:70132429-70132430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs201566952	chr4:70132449-70132450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566979250	chr4:70132479-70132480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555703188	chr4:70132489-70132490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545791148	chr4:70132556-70132557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569315978	chr4:70132567-70132568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370663603	chr4:70132571-70132572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374572866	chr4:70132576-70132577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538111547	chr4:70132594-70132595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368765012	chr4:70132623-70132624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374941816	chr4:70132639-70132640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558072845	chr4:70132648-70132649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs578122745	chr4:70132650-70132651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540500416	chr4:70132651-70132652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554225313	chr4:70132677-70132678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556188643	chr4:70132688-70132689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7697812	chr4:70132702-70132703	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs543165478	chr4:70132715-70132716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541701178	chr4:70132817-70132818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562823731	chr4:70132818-70132819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186472904	chr4:70132821-70132822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141426223	chr4:70132832-70132833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527813786	chr4:70132842-70132843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565078159	chr4:70132853-70132854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527458248	chr4:70132870-70132871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547307728	chr4:70132898-70132899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561150031	chr4:70132914-70132915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189756246	chr4:70132923-70132924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150361872	chr4:70133106-70133107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183242309	chr4:70133111-70133112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7670009	chr4:70133118-70133119	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs551637283	chr4:70133132-70133133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559220907	chr4:70133134-70133135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188170852	chr4:70133146-70133147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113529979	chr4:70133153-70133154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs193070568	chr4:70133155-70133156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375174315	chr4:70133187-70133188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536704571	chr4:70133192-70133193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556734387	chr4:70133193-70133194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563944155	chr4:70135200-70135201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116053189	chr4:70135229-70135230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192692219	chr4:70135253-70135254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546183361	chr4:70135270-70135271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560801854	chr4:70135294-70135295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116819418	chr4:70135298-70135299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs111941774	chr4:70135299-70135300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561873174	chr4:70135341-70135342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184141248	chr4:70135344-70135345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201149567	chr4:70135363-70135364	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21215367	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70132400-70133000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr4:70132400-70133200	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr4:70132800-70133200	Enhancers	H9 Cell Line	embryonic stem cell
4	chr4:70135200-70135600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr4:70174000-70176000	Enhancers	Stomach Mucosa	stomach
6	chr4:70174200-70175000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:70174400-70174600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:70174400-70176400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr4:70174600-70175400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:70174600-70175400	Enhancers	HepG2	liver
11	chr4:70174600-70176200	Enhancers	Fetal Intestine Large	intestine
12	chr4:70174600-70176200	Enhancers	Fetal Intestine Small	intestine
13	chr4:70174800-70175200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr4:70174800-70176600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr4:70175000-70175800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr4:70175000-70176000	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr4:70175800-70176800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:70176000-70181400	Weak transcription	Stomach Mucosa	stomach
19	chr4:70176600-70178600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr4:70176800-70183400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:70178600-70178800	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr4:70178800-70179000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr4:70181400-70181800	Enhancers	Stomach Mucosa	stomach
24	chr4:70181800-70183400	Weak transcription	Stomach Mucosa	stomach
25	chr4:70183400-70183600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr4:70183400-70183800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:70183400-70184000	Enhancers	Stomach Mucosa	stomach
28	chr4:70183600-70183800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr4:70183800-70186600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr4:70183800-70187600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:70184000-70186600	Weak transcription	Stomach Mucosa	stomach
32	chr4:70186600-70187200	Enhancers	HSMMtube	muscle
33	chr4:70186600-70188400	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr4:70186600-70188400	Enhancers	Fetal Intestine Large	intestine
35	chr4:70186600-70189600	Enhancers	Stomach Mucosa	stomach
36	chr4:70186800-70187400	Enhancers	K562	blood
37	chr4:70186800-70187600	Enhancers	HSMM	muscle
38	chr4:70186800-70187800	Enhancers	Esophagus	oesophagus
39	chr4:70186800-70188000	Enhancers	Gastric	stomach
40	chr4:70186800-70188000	Enhancers	Pancreas	Pancrea
41	chr4:70186800-70188400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr4:70187000-70187400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:70187000-70187600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr4:70187000-70187800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:70187000-70187800	Enhancers	Liver	Liver
46	chr4:70187000-70188000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:70187000-70188400	Enhancers	HMEC	breast
48	chr4:70187200-70187800	Flanking Active TSS	HSMMtube	muscle
49	chr4:70187200-70188400	Enhancers	Muscle Satellite Cultured Cells	--
50	chr4:70187400-70188000	Enhancers	Skeletal Muscle Male	skeletal muscle

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