Variant report

Variant	esv1850010
Chromosome Location	chr4:70094226-70236231
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:705)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:705 , 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	chr4:70105523-70105754	K562	blood:	n/a	n/a
2	ARID3A	chr4:70106482-70106878	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70105540-70105900	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70210667-70210694	HepG2	liver:	n/a	n/a
5	ATF1	chr4:70175307-70175700	K562	blood:	n/a	n/a
6	ATF1	chr4:70105493-70105808	K562	blood:	n/a	n/a
7	ATF1	chr4:70187845-70188142	K562	blood:	n/a	n/a
8	BACH1	chr4:70097393-70097475	K562	blood:	n/a	n/a
9	BHLHE40	chr4:70105574-70105707	K562	blood:	n/a	n/a
10	BHLHE40	chr4:70209675-70209715	K562	blood:	n/a	n/a
11	CBX3	chr4:70175213-70175493	K562	blood:	n/a	n/a
12	CCNT2	chr4:70105530-70105702	K562	blood:	n/a	n/a
13	CEBPB	chr4:70148592-70148690	A549	lung:	n/a	chr4:70148623-70148634
14	CEBPB	chr4:70148603-70148719	H1-hESC	embryonic stem cell:	n/a	chr4:70148623-70148634
15	CEBPB	chr4:70105462-70105782	K562	blood:	n/a	n/a
16	CEBPB	chr4:70211562-70211766	HepG2	liver:	n/a	chr4:70211703-70211714
17	CEBPB	chr4:70209480-70209728	K562	blood:	n/a	n/a
18	CEBPB	chr4:70118972-70119263	HepG2	liver:	n/a	chr4:70119163-70119176
19	CEBPB	chr4:70221057-70221267	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:70107631-70107834	A549	lung:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
21	CEBPB	chr4:70226229-70226403	HepG2	liver:	n/a	chr4:70226280-70226289 chr4:70226280-70226291
22	CEBPB	chr4:70107648-70107863	HepG2	liver:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
23	CEBPB	chr4:70105548-70105721	K562	blood:	n/a	n/a
24	CEBPB	chr4:70106514-70106708	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:70148545-70148642	K562	blood:	n/a	chr4:70148623-70148634
26	CEBPD	chr4:70105414-70105831	K562	blood:	n/a	n/a
27	CTCF	chr4:70201360-70201510	GM12874	blood:	n/a	n/a
28	CTCF	chr4:70183700-70183850	GM12874	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
29	CTCF	chr4:70201360-70201510	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr4:70134460-70134610	HepG2	liver:	n/a	n/a
31	CTCF	chr4:70201227-70201509	A549	lung:	n/a	n/a
32	CTCF	chr4:70183760-70183910	BE2_C	brain:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
33	CTCF	chr4:70174564-70174638	GM20000	blood:	n/a	n/a
34	CTCF	chr4:70097033-70097046	GM13977	blood:	n/a	n/a
35	CTCF	chr4:70201320-70201470	GM12874	blood:	n/a	n/a
36	CTCF	chr4:70189120-70189270	HepG2	liver:	n/a	n/a
37	CTCF	chr4:70183680-70183905	GM20000	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
38	CTCF	chr4:70183740-70183890	GM12872	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
39	CTCF	chr4:70201340-70201490	HPF	lung:	n/a	n/a
40	CTCF	chr4:70183739-70183847	MCF-7	breast:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
41	CTCF	chr4:70183580-70183730	HFF	foreskin:	n/a	n/a
42	CTCF	chr4:70183700-70183850	GM12865	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
43	CTCF	chr4:70201400-70201550	HAc	cerebellar:	n/a	n/a
44	CTCF	chr4:70183700-70183850	HCFaa	heart:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
45	CTCF	chr4:70187137-70187165	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:70201334-70201482	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:70201321-70201465	LNCaP	prostate:	n/a	n/a
48	CTCF	chr4:70189200-70189350	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr4:70097000-70097025	GM13977	blood:	n/a	n/a
50	CTCF	chr4:70134463-70134574	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70155747-70155797	SK-N-SH_RA	brain:	n/a
2	chr4:70155747-70155797	AG04449	skin:	fetal
3	chr4:70155747-70155797	A549	lung:	n/a
4	chr4:70155747-70155797	GM12891	blood:	n/a
5	chr4:70155747-70155797	NHBE	bronchial:	n/a
6	chr4:70155747-70155797	GM06990	blood:	n/a
7	chr4:70155747-70155797	SK-N-SH	brain:	n/a
8	chr4:70155747-70155797	Caco-2	colon:	n/a
9	chr4:70155747-70155797	NHDF-neo	bronchial:	n/a
10	chr4:70155747-70155797	HUVEC	blood vessel:	n/a
11	chr4:70155747-70155797	HRPEpiC	eye:	n/a
12	chr4:70155747-70155797	PANC-1	pancreas:	n/a
13	chr4:70155747-70155797	K562	blood:	n/a
14	chr4:70155747-70155797	HRCEpiC	kidney:	n/a
15	chr4:70155747-70155797	AG09319	gingival:	n/a
16	chr4:70155747-70155797	H1-hESC	embryonic stem cell:	embryo
17	chr4:70155747-70155797	SKMC	muscle:	n/a
18	chr4:70155747-70155797	HPAEpiC	pulmonary alveolar:	n/a
19	chr4:70155747-70155797	AG09309	skin:	n/a
20	chr4:70155747-70155797	NB4	blood:	n/a
21	chr4:70155747-70155797	NT2-D1	testis:	n/a
22	chr4:70155747-70155797	HL-60	blood:	n/a
23	chr4:70155747-70155797	AG10803	skin:	n/a
24	chr4:70155747-70155797	T-47D	breast:	n/a
25	chr4:70155747-70155797	GM19239	blood:	n/a
26	chr4:70155747-70155797	ProgFib	skin:	n/a
27	chr4:70155747-70155797	AG04450	lung:	fetal
28	chr4:70155747-70155797	HCT-116	colon:	n/a
29	chr4:70155747-70155797	U87	brain:	n/a
30	chr4:70155747-70155797	BE2_C	brain:	n/a
31	chr4:70155747-70155797	ovcar-3	ovarian:	n/a
32	chr4:70155747-70155797	PFSK-1	brain:	n/a
33	chr4:70155747-70155797	MCF-7	breast:	n/a
34	chr4:70155747-70155797	HNPCEpiC	eye:	n/a
35	chr4:70155747-70155797	SK-N-MC	brain:	n/a
36	chr4:70155747-70155797	Hela-S3	cervix:	n/a
37	chr4:70155747-70155797	RPTEC	kidney:	n/a
38	chr4:70155747-70155797	HCM	heart:	n/a
39	chr4:70155747-70155797	CMK	blood:	n/a
40	chr4:70155747-70155797	GM12892	blood:	n/a
41	chr4:70155747-70155797	HAEpiC	amniotic membrane:	n/a
42	chr4:70155747-70155797	IMR90	lung:	fetal
43	chr4:70155747-70155797	SAEC	small airway:	n/a
44	chr4:70155747-70155797	HCPEpiC	choroid plexus:	n/a
45	chr4:70155747-70155797	HEK293	kidney:	embryo
46	chr4:70155747-70155797	BJ	skin:	n/a
47	chr4:70155747-70155797	LNCaP	prostate:	n/a
48	chr4:70155747-70155797	HRE	kidney:	n/a
49	chr4:70155747-70155797	HMEC	breast:	n/a
50	chr4:70155747-70155797	AoSMC	blood vessel:	n/a

(count:6 , 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	chr4:70183605..70184238-chr4:70482598..70483352,3	MCF-7	breast:
4	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
5	chr4:69789542..69791043-chr4:70152702..70154403,2	MCF-7	breast:
6	chr4:70183340..70184245-chr4:70482427..70483057,3	MCF-7	breast:

No data

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

Extended variants
information (count: 1772 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs36182222	chr4:70104603-70104604	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75924320	chr4:70104613-70104614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113476750	chr4:70104626-70104627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74971482	chr4:70104643-70104644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76804954	chr4:70104646-70104647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571375061	chr4:70104648-70104649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78948827	chr4:70104654-70104655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536668970	chr4:70104662-70104663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547464048	chr4:70104689-70104690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550113020	chr4:70104690-70104691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370251737	chr4:70104692-70104693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374050348	chr4:70104705-70104706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536182909	chr4:70104722-70104723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78434970	chr4:70104724-70104725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76688588	chr4:70104738-70104739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567232436	chr4:70104752-70104753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75213908	chr4:70104769-70104770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs80090470	chr4:70104770-70104771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79598421	chr4:70104778-70104779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78891139	chr4:70104792-70104793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183337122	chr4:70104804-70104805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538074545	chr4:70104808-70104809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187514094	chr4:70104811-70104812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148566320	chr4:70104812-70104813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191041740	chr4:70104820-70104821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552921137	chr4:70104833-70104834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12499805	chr4:70104853-70104854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs202011835	chr4:70104854-70104855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs71204086	chr4:70104860-70104861	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs149833023	chr4:70104861-70104862	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs368876511	chr4:70104865-70104866	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs116709341	chr4:70104871-70104872	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs542936301	chr4:70104888-70104889	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs562662359	chr4:70104898-70104899	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs531494097	chr4:70104900-70104901	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs545226881	chr4:70104923-70104924	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs375287972	chr4:70104942-70104943	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs572978774	chr4:70104952-70104953	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs182808063	chr4:70104974-70104975	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs538421930	chr4:70105009-70105010	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs188437448	chr4:70105013-70105014	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs72501239	chr4:70105054-70105055	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs192902405	chr4:70105106-70105107	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs201589372	chr4:70105110-70105111	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs529681210	chr4:70105129-70105130	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs184649841	chr4:70105152-70105153	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs187840356	chr4:70105169-70105170	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs538386795	chr4:70105232-70105233	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs192419201	chr4:70105261-70105262	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs144025188	chr4:70105285-70105286	Enhancers	TF binding region	1 gene(s)	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:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70104600-70106600	Enhancers	Fetal Intestine Large	intestine
2	chr4:70105000-70106600	Enhancers	Fetal Intestine Small	intestine
3	chr4:70105000-70106600	Enhancers	HepG2	liver
4	chr4:70105200-70106000	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr4:70105200-70106400	Enhancers	Duodenum Mucosa	Duodenum
6	chr4:70105200-70106400	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr4:70105200-70106600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:70105200-70106800	Enhancers	Stomach Mucosa	stomach
9	chr4:70105400-70105800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr4:70105400-70106200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr4:70106200-70106600	Enhancers	Small Intestine	intestine
12	chr4:70106600-70108400	Weak transcription	HepG2	liver
13	chr4:70108400-70108800	Enhancers	HepG2	liver
14	chr4:70111600-70112000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:70112000-70113400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:70113400-70114000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:70132400-70133000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr4:70132400-70133200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:70132800-70133200	Enhancers	H9 Cell Line	embryonic stem cell
20	chr4:70135200-70135600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr4:70174000-70176000	Enhancers	Stomach Mucosa	stomach
22	chr4:70174200-70175000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:70174400-70174600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:70174400-70176400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr4:70174600-70175400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:70174600-70175400	Enhancers	HepG2	liver
27	chr4:70174600-70176200	Enhancers	Fetal Intestine Large	intestine
28	chr4:70174600-70176200	Enhancers	Fetal Intestine Small	intestine
29	chr4:70174800-70175200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr4:70174800-70176600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr4:70175000-70175800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr4:70175000-70176000	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr4:70175800-70176800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr4:70176000-70181400	Weak transcription	Stomach Mucosa	stomach
35	chr4:70176600-70178600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr4:70176800-70183400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:70178600-70178800	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr4:70178800-70179000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr4:70181400-70181800	Enhancers	Stomach Mucosa	stomach
40	chr4:70181800-70183400	Weak transcription	Stomach Mucosa	stomach
41	chr4:70183400-70183600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr4:70183400-70183800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:70183400-70184000	Enhancers	Stomach Mucosa	stomach
44	chr4:70183600-70183800	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr4:70183800-70186600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr4:70183800-70187600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr4:70184000-70186600	Weak transcription	Stomach Mucosa	stomach
48	chr4:70186600-70187200	Enhancers	HSMMtube	muscle
49	chr4:70186600-70188400	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr4:70186600-70188400	Enhancers	Fetal Intestine Large	intestine

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