Variant report

Variant	nsv879406
Chromosome Location	chr4:70107295-70234419
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70210667-70210694	HepG2	liver:	n/a	n/a
2	ATF1	chr4:70175307-70175700	K562	blood:	n/a	n/a
3	ATF1	chr4:70187845-70188142	K562	blood:	n/a	n/a
4	BHLHE40	chr4:70209675-70209715	K562	blood:	n/a	n/a
5	CBX3	chr4:70175213-70175493	K562	blood:	n/a	n/a
6	CEBPB	chr4:70107631-70107834	A549	lung:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
7	CEBPB	chr4:70221057-70221267	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:70226229-70226403	HepG2	liver:	n/a	chr4:70226280-70226289 chr4:70226280-70226291
9	CEBPB	chr4:70148545-70148642	K562	blood:	n/a	chr4:70148623-70148634
10	CEBPB	chr4:70107648-70107863	HepG2	liver:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
11	CEBPB	chr4:70118972-70119263	HepG2	liver:	n/a	chr4:70119163-70119176
12	CEBPB	chr4:70209480-70209728	K562	blood:	n/a	n/a
13	CEBPB	chr4:70148592-70148690	A549	lung:	n/a	chr4:70148623-70148634
14	CEBPB	chr4:70211562-70211766	HepG2	liver:	n/a	chr4:70211703-70211714
15	CEBPB	chr4:70148603-70148719	H1-hESC	embryonic stem cell:	n/a	chr4:70148623-70148634
16	CTCF	chr4:70183600-70183750	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr4:70134440-70134590	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr4:70189180-70189330	K562	blood:	n/a	n/a
19	CTCF	chr4:70183493-70184153	A549	lung:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
20	CTCF	chr4:70183698-70183913	Kidney_OC	kidney:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
21	CTCF	chr4:70201320-70201470	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr4:70183600-70183750	HVMF	connective:	n/a	n/a
23	CTCF	chr4:70183780-70183930	GM12872	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
24	CTCF	chr4:70201079-70201181	Lung_OC	lung:	n/a	n/a
25	CTCF	chr4:70187126-70187161	MCF-7	breast:	n/a	n/a
26	CTCF	chr4:70189020-70189170	GM12864	blood:	n/a	n/a
27	CTCF	chr4:70183720-70183870	GM06990	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
28	CTCF	chr4:70183692-70183938	LNCaP	prostate:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
29	CTCF	chr4:70183800-70183950	HMEC	breast:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
30	CTCF	chr4:70183693-70183935	GM10248	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
31	CTCF	chr4:70153377-70153405	LNCaP	prostate:	n/a	n/a
32	CTCF	chr4:70183585-70183941	A549	lung:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
33	CTCF	chr4:70183639-70183899	Gliobla	brain:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
34	CTCF	chr4:70183740-70183890	HMF	breast:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
35	CTCF	chr4:70183720-70183870	NHEK	skin:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
36	CTCF	chr4:70183682-70183964	HepG2	liver:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
37	CTCF	chr4:70183720-70183870	GM12864	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
38	CTCF	chr4:70183740-70183890	AG10803	skin:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
39	CTCF	chr4:70183929-70183931	GM10266	blood:	n/a	n/a
40	CTCF	chr4:70134443-70134568	Gliobla	brain:	n/a	n/a
41	CTCF	chr4:70183800-70183950	RPTEC	kidney:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
42	CTCF	chr4:70189160-70189310	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:70189180-70189330	GM06990	blood:	n/a	n/a
44	CTCF	chr4:70183687-70183889	HepG2	liver:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
45	CTCF	chr4:70183485-70184174	SK-N-SH	brain:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
46	CTCF	chr4:70201320-70201470	GM12872	blood:	n/a	n/a
47	CTCF	chr4:70183700-70183850	GM12874	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
48	CTCF	chr4:70201422-70201428	ProgFib	skin:	n/a	n/a
49	CTCF	chr4:70201260-70201460	IMR90	lung:	n/a	n/a
50	CTCF	chr4:70183800-70183950	MCF-7	breast:	n/a	chr4:70183815-70183833 chr4:70183817-70183838

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70155747-70155797	AG04449	skin:	fetal
2	chr4:70155747-70155797	PANC-1	pancreas:	n/a
3	chr4:70155747-70155797	HRE	kidney:	n/a
4	chr4:70155747-70155797	HL-60	blood:	n/a
5	chr4:70155747-70155797	GM12878	blood:	n/a
6	chr4:70155747-70155797	HNPCEpiC	eye:	n/a
7	chr4:70155747-70155797	Hela-S3	cervix:	n/a
8	chr4:70155747-70155797	BJ	skin:	n/a
9	chr4:70155747-70155797	AoSMC	blood vessel:	n/a
10	chr4:70155747-70155797	NHBE	bronchial:	n/a
11	chr4:70155747-70155797	NH-A	brain:	n/a
12	chr4:70155747-70155797	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:70155747-70155797	HUVEC	blood vessel:	n/a
14	chr4:70155747-70155797	HAEpiC	amniotic membrane:	n/a
15	chr4:70155747-70155797	HCT-116	colon:	n/a
16	chr4:70155747-70155797	HIPEpiC	eye:	n/a
17	chr4:70155747-70155797	H1-hESC	embryonic stem cell:	embryo
18	chr4:70155747-70155797	U87	brain:	n/a
19	chr4:70155747-70155797	ECC-1	luminal epithelium:	n/a
20	chr4:70155747-70155797	PrEC	prostate:	n/a
21	chr4:70155747-70155797	AG04450	lung:	fetal
22	chr4:70155747-70155797	SKMC	muscle:	n/a
23	chr4:70155747-70155797	IMR90	lung:	fetal
24	chr4:70155747-70155797	AG10803	skin:	n/a
25	chr4:70155747-70155797	HCPEpiC	choroid plexus:	n/a
26	chr4:70155747-70155797	HCF	heart:	n/a
27	chr4:70155747-70155797	PFSK-1	brain:	n/a
28	chr4:70155747-70155797	NHDF-neo	bronchial:	n/a
29	chr4:70155747-70155797	T-47D	breast:	n/a
30	chr4:70155747-70155797	SK-N-SH	brain:	n/a
31	chr4:70155747-70155797	RPTEC	kidney:	n/a
32	chr4:70155747-70155797	MCF-7	breast:	n/a
33	chr4:70155747-70155797	HMEC	breast:	n/a
34	chr4:70155747-70155797	HRCEpiC	kidney:	n/a
35	chr4:70155747-70155797	Jurkat	blood:	n/a
36	chr4:70155747-70155797	LNCaP	prostate:	n/a
37	chr4:70155747-70155797	SK-N-SH_RA	brain:	n/a
38	chr4:70155747-70155797	HEK293	kidney:	embryo
39	chr4:70155747-70155797	Caco-2	colon:	n/a
40	chr4:70155747-70155797	ProgFib	skin:	n/a
41	chr4:70155747-70155797	GM06990	blood:	n/a
42	chr4:70155747-70155797	Hepatocyte	liver:	n/a
43	chr4:70155747-70155797	HRPEpiC	eye:	n/a
44	chr4:70155747-70155797	SAEC	small airway:	n/a
45	chr4:70155747-70155797	HCM	heart:	n/a
46	chr4:70155747-70155797	GM12892	blood:	n/a
47	chr4:70155747-70155797	NT2-D1	testis:	n/a
48	chr4:70155747-70155797	ovcar-3	ovarian:	n/a
49	chr4:70155747-70155797	CMK	blood:	n/a
50	chr4:70155747-70155797	HepG2	liver:	n/a

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

Variant related genes	Relation type
ENSG00000251691	TF binding region
ENSG00000249763	TF binding region
ENSG00000250612	TF binding region
UGT2B28	TF binding region
ENSG00000251691	CpG island
ENSG00000249763	CpG island
ENSG00000250612	CpG island
UGT2B28	CpG island
ENSG00000198277	chromatin interactions

Extended variants
information (count: 1607 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1607 , 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	rs13148971	chr4:70107295-70107296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs13128147	chr4:70107299-70107300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs13117922	chr4:70107306-70107307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13128161	chr4:70107330-70107331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13134798	chr4:70107352-70107353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs13134811	chr4:70107386-70107387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs13128367	chr4:70107401-70107402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554920755	chr4:70107402-70107403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs13118154	chr4:70107409-70107410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs56002130	chr4:70107454-70107455	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs181678692	chr4:70107478-70107479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563904635	chr4:70107493-70107494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113782671	chr4:70107505-70107506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71618636	chr4:70107506-70107507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs71618635	chr4:70107519-70107520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs71618634	chr4:70107527-70107528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532628322	chr4:70107529-70107530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546290390	chr4:70107552-70107553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71618633	chr4:70107557-70107558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs71618632	chr4:70107565-70107566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs58846646	chr4:70107583-70107584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs71618631	chr4:70107592-70107593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559899808	chr4:70107600-70107601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562339799	chr4:70107633-70107634	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs71618630	chr4:70107642-70107643	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs546387844	chr4:70107648-70107649	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs548565686	chr4:70107649-70107650	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs562733595	chr4:70107651-70107652	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs71618629	chr4:70107666-70107667	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs71618628	chr4:70107672-70107673	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs71618627	chr4:70107679-70107680	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs71618626	chr4:70107707-70107708	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs530868820	chr4:70107708-70107709	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs71618625	chr4:70107717-70107718	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs13434803	chr4:70107743-70107744	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs71598099	chr4:70107746-70107747	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs71618624	chr4:70107837-70107838	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs187180691	chr4:70107908-70107909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71618623	chr4:70107922-70107923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71618622	chr4:70107949-70107950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71618621	chr4:70107954-70107955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560614123	chr4:70107957-70107958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190759753	chr4:70107966-70107967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566567975	chr4:70107982-70107983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs71641443	chr4:70107986-70107987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529712953	chr4:70107988-70107989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs180811168	chr4:70108002-70108003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546229978	chr4:70108014-70108015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71618620	chr4:70108022-70108023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189852243	chr4:70108023-70108024	Weak transcription	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioblastoma multiforme	21510904	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70106600-70108400	Weak transcription	HepG2	liver
2	chr4:70108400-70108800	Enhancers	HepG2	liver
3	chr4:70111600-70112000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:70112000-70113400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:70113400-70114000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:70132400-70133000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:70132400-70133200	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr4:70132800-70133200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr4:70135200-70135600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr4:70174000-70176000	Enhancers	Stomach Mucosa	stomach
11	chr4:70174200-70175000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr4:70174400-70174600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr4:70174400-70176400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr4:70174600-70175400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:70174600-70175400	Enhancers	HepG2	liver
16	chr4:70174600-70176200	Enhancers	Fetal Intestine Large	intestine
17	chr4:70174600-70176200	Enhancers	Fetal Intestine Small	intestine
18	chr4:70174800-70175200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr4:70174800-70176600	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr4:70175000-70175800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:70175000-70176000	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr4:70175800-70176800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:70176000-70181400	Weak transcription	Stomach Mucosa	stomach
24	chr4:70176600-70178600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr4:70176800-70183400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:70178600-70178800	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr4:70178800-70179000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr4:70181400-70181800	Enhancers	Stomach Mucosa	stomach
29	chr4:70181800-70183400	Weak transcription	Stomach Mucosa	stomach
30	chr4:70183400-70183600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr4:70183400-70183800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr4:70183400-70184000	Enhancers	Stomach Mucosa	stomach
33	chr4:70183600-70183800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr4:70183800-70186600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr4:70183800-70187600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:70184000-70186600	Weak transcription	Stomach Mucosa	stomach
37	chr4:70186600-70187200	Enhancers	HSMMtube	muscle
38	chr4:70186600-70188400	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr4:70186600-70188400	Enhancers	Fetal Intestine Large	intestine
40	chr4:70186600-70189600	Enhancers	Stomach Mucosa	stomach
41	chr4:70186800-70187400	Enhancers	K562	blood
42	chr4:70186800-70187600	Enhancers	HSMM	muscle
43	chr4:70186800-70187800	Enhancers	Esophagus	oesophagus
44	chr4:70186800-70188000	Enhancers	Gastric	stomach
45	chr4:70186800-70188000	Enhancers	Pancreas	Pancrea
46	chr4:70186800-70188400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr4:70187000-70187400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr4:70187000-70187600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr4:70187000-70187800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:70187000-70187800	Enhancers	Liver	Liver

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