Variant report

Variant	nsv1028908
Chromosome Location	chr4:131137147-131331018
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:713)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:713 , 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	BACH1	chr4:131214873-131215274	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:131241802-131241814	K562	blood:	n/a	n/a
3	BHLHE40	chr4:131154596-131154980	GM12878	blood:	n/a	n/a
4	BRCA1	chr4:131193213-131193277	GM12878	blood:	n/a	n/a
5	BRCA1	chr4:131233006-131233018	GM12878	blood:	n/a	n/a
6	CEBPB	chr4:131167751-131167960	IMR90	lung:	n/a	n/a
7	CEBPB	chr4:131209133-131209333	IMR90	lung:	n/a	chr4:131209155-131209166 chr4:131209272-131209285 chr4:131209272-131209285 chr4:131209155-131209164
8	CEBPB	chr4:131216164-131216412	A549	lung:	n/a	chr4:131216270-131216283 chr4:131216271-131216282
9	CEBPB	chr4:131216198-131216409	HepG2	liver:	n/a	chr4:131216270-131216283 chr4:131216271-131216282
10	CEBPB	chr4:131316973-131317483	IMR90	lung:	n/a	n/a
11	CTCF	chr4:131324520-131324670	HCT-116	colon:	n/a	n/a
12	CTCF	chr4:131257810-131258084	Gliobla	brain:	n/a	n/a
13	CTCF	chr4:131257840-131257990	NB4	blood:	n/a	n/a
14	CTCF	chr4:131227920-131228070	MCF-7	breast:	n/a	n/a
15	CTCF	chr4:131257900-131258050	GM12870	blood:	n/a	n/a
16	CTCF	chr4:131280749-131280995	K562	blood:	n/a	chr4:131280885-131280903 chr4:131280887-131280908
17	CTCF	chr4:131257860-131258010	HCM	heart:	n/a	n/a
18	CTCF	chr4:131280840-131280990	WI-38	lung:	n/a	chr4:131280885-131280903 chr4:131280887-131280908
19	CTCF	chr4:131258195-131258213	GM19239	blood:	n/a	n/a
20	CTCF	chr4:131178540-131178690	HA-sp	spinal cord:	n/a	n/a
21	CTCF	chr4:131257880-131258030	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr4:131324506-131324621	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:131258160-131258310	GM12866	blood:	n/a	n/a
24	CTCF	chr4:131257867-131258026	HepG2	liver:	n/a	n/a
25	CTCF	chr4:131280752-131280978	HepG2	liver:	n/a	chr4:131280885-131280903 chr4:131280887-131280908
26	CTCF	chr4:131280840-131280990	AoAF	blood vessel:	n/a	chr4:131280885-131280903 chr4:131280887-131280908
27	CTCF	chr4:131280800-131280950	HEEpiC	esophagus:	n/a	chr4:131280885-131280903 chr4:131280887-131280908
28	CTCF	chr4:131178540-131178690	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr4:131257845-131258038	GM10266	blood:	n/a	n/a
30	CTCF	chr4:131178620-131178770	NHEK	skin:	n/a	n/a
31	CTCF	chr4:131257400-131257550	BE2_C	brain:	n/a	n/a
32	CTCF	chr4:131257840-131257990	AG09319	gingival:	n/a	n/a
33	CTCF	chr4:131178360-131178510	HCM	heart:	n/a	n/a
34	CTCF	chr4:131257880-131258030	GM12864	blood:	n/a	n/a
35	CTCF	chr4:131178680-131178830	AG04450	lung:	n/a	n/a
36	CTCF	chr4:131257827-131258046	GM10248	blood:	n/a	n/a
37	CTCF	chr4:131257880-131258030	GM12871	blood:	n/a	n/a
38	CTCF	chr4:131258260-131258410	NHEK	skin:	n/a	n/a
39	CTCF	chr4:131280780-131280930	BE2_C	brain:	n/a	chr4:131280885-131280903 chr4:131280887-131280908
40	CTCF	chr4:131227860-131228010	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr4:131227899-131227931	GM20000	blood:	n/a	n/a
42	CTCF	chr4:131280800-131280950	SK-N-SH_RA	brain:	n/a	chr4:131280885-131280903 chr4:131280887-131280908
43	CTCF	chr4:131257900-131258050	Caco-2	colon:	n/a	n/a
44	CTCF	chr4:131257820-131257970	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr4:131280820-131280970	HRPEpiC	eye:	n/a	chr4:131280885-131280903 chr4:131280887-131280908
46	CTCF	chr4:131324539-131324596	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:131280860-131281010	HCT-116	colon:	n/a	chr4:131280885-131280903 chr4:131280887-131280908
48	CTCF	chr4:131257860-131258010	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr4:131257880-131258030	HCM	heart:	n/a	n/a
50	CTCF	chr4:131227960-131228110	GM12866	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:131254713-131254763	NHDF-neo	bronchial:	n/a
2	chr4:131254713-131254763	AoSMC	blood vessel:	n/a
3	chr4:131254713-131254763	A549	lung:	n/a
4	chr4:131254713-131254763	H1-hESC	embryonic stem cell:	embryo
5	chr4:131254713-131254763	SK-N-SH	brain:	n/a
6	chr4:131254713-131254763	GM12878	blood:	n/a
7	chr4:131254713-131254763	BJ	skin:	n/a
8	chr4:131254713-131254763	ProgFib	skin:	n/a
9	chr4:131254713-131254763	AG04449	skin:	fetal
10	chr4:131254713-131254763	SAEC	small airway:	n/a
11	chr4:131254713-131254763	HCPEpiC	choroid plexus:	n/a
12	chr4:131254713-131254763	HEEpiC	esophagus:	n/a
13	chr4:131254713-131254763	IMR90	lung:	fetal
14	chr4:131254713-131254763	T-47D	breast:	n/a
15	chr4:131254713-131254763	HPAEpiC	pulmonary alveolar:	n/a
16	chr4:131254713-131254763	NHBE	bronchial:	n/a
17	chr4:131254713-131254763	HRE	kidney:	n/a
18	chr4:131254713-131254763	HUVEC	blood vessel:	n/a
19	chr4:131254713-131254763	ECC-1	luminal epithelium:	n/a
20	chr4:131254713-131254763	MCF10A-Er-Src	breast:	n/a
21	chr4:131254713-131254763	HNPCEpiC	eye:	n/a
22	chr4:131254713-131254763	AG09309	skin:	n/a
23	chr4:131254713-131254763	CMK	blood:	n/a
24	chr4:131254713-131254763	K562	blood:	n/a
25	chr4:131254713-131254763	HAEpiC	amniotic membrane:	n/a
26	chr4:131254713-131254763	PANC-1	pancreas:	n/a
27	chr4:131254713-131254763	BE2_C	brain:	n/a
28	chr4:131254713-131254763	MCF-7	breast:	n/a
29	chr4:131254713-131254763	RPTEC	kidney:	n/a
30	chr4:131254713-131254763	AG09319	gingival:	n/a
31	chr4:131254713-131254763	PFSK-1	brain:	n/a
32	chr4:131254713-131254763	HL-60	blood:	n/a
33	chr4:131254713-131254763	Hela-S3	cervix:	n/a
34	chr4:131254713-131254763	GM19239	blood:	n/a
35	chr4:131254713-131254763	U87	brain:	n/a
36	chr4:131254713-131254763	GM06990	blood:	n/a
37	chr4:131254713-131254763	NH-A	brain:	n/a
38	chr4:131254713-131254763	NT2-D1	testis:	n/a
39	chr4:131254713-131254763	AG04450	lung:	fetal
40	chr4:131254713-131254763	SKMC	muscle:	n/a
41	chr4:131254713-131254763	SK-N-MC	brain:	n/a
42	chr4:131254713-131254763	HMEC	breast:	n/a
43	chr4:131254713-131254763	HCT-116	colon:	n/a
44	chr4:131254713-131254763	ovcar-3	ovarian:	n/a
45	chr4:131254713-131254763	HCM	heart:	n/a
46	chr4:131254713-131254763	Hepatocyte	liver:	n/a
47	chr4:131254713-131254763	PrEC	prostate:	n/a
48	chr4:131254713-131254763	SK-N-SH_RA	brain:	n/a
49	chr4:131254713-131254763	HRCEpiC	kidney:	n/a
50	chr4:131254713-131254763	HIPEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:131162135..131163793-chr4:131168250..131170399,2	K562	blood:
2	chr4:131283086..131285023-chr4:131287363..131290249,2	MCF-7	breast:
3	chr4:131149586..131151666-chr4:131154297..131156397,2	K562	blood:
4	chr19:7708632..7709166-chr4:131266218..131266718,2	NB4	blood:
5	chr4:131162293..131164419-chr4:131168250..131170344,2	K562	blood:
6	chr13:97378483..97379144-chr4:131166728..131167230,2	MCF-7	breast:
7	chr4:131162293..131164419-chr4:131168250..131170344,2	K562	blood:
8	chr4:131242207..131244895-chr4:131247047..131249107,2	K562	blood:
9	chr4:131149586..131151666-chr4:131154297..131156397,2	K562	blood:
10	chr4:131153992..131157908-chr4:131192612..131195351,3	K562	blood:
11	chr4:131242207..131244895-chr4:131247047..131249107,2	K562	blood:
12	chr4:131153992..131157908-chr4:131192612..131195351,3	K562	blood:
13	chr4:131283086..131285023-chr4:131287363..131290249,2	MCF-7	breast:
14	chr4:131162135..131163793-chr4:131168250..131170399,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf33-2	chr4:131307228-131307526	XLOC_003688
2	lnc-C4orf33-2	chr4:131297384-131297714	XLOC_003688

No data

Variant related genes	Relation type
ENSG00000251326	TF binding region
ENSG00000251326	CpG island

Extended variants
information (count: 2529 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2529 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530218540	chr4:131137465-131137466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552246529	chr4:131137498-131137499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548743438	chr4:131137513-131137514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192993933	chr4:131137515-131137516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527692545	chr4:131137530-131137531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1353060	chr4:131137565-131137566	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs570672759	chr4:131137566-131137567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538175818	chr4:131137579-131137580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556063882	chr4:131137597-131137598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557447198	chr4:131137616-131137617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567953969	chr4:131137649-131137650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150662158	chr4:131137754-131137755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553452364	chr4:131137760-131137761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs386679508	chr4:131137761-131137762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79324046	chr4:131137762-131137763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1024019	chr4:131137793-131137794	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs577442785	chr4:131137834-131137835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527874150	chr4:131137837-131137838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563065863	chr4:131137843-131137844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562438613	chr4:131137846-131137847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79745482	chr4:131137888-131137889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542299132	chr4:131137910-131137911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368134260	chr4:131137938-131137939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560590694	chr4:131137939-131137940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527653878	chr4:131137964-131137965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543816773	chr4:131137965-131137966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139920177	chr4:131137992-131137993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1994847	chr4:131138036-131138037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531497170	chr4:131138103-131138104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550058276	chr4:131138172-131138173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567866150	chr4:131138192-131138193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563611614	chr4:131138194-131138195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116247855	chr4:131138815-131138816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs58851838	chr4:131138843-131138844	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs565582572	chr4:131138850-131138851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551253549	chr4:131138885-131138886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs199971106	chr4:131138893-131138894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539153035	chr4:131138921-131138922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551467092	chr4:131138951-131138952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143967502	chr4:131138958-131138959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181404034	chr4:131138991-131138992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556863141	chr4:131139026-131139027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186339330	chr4:131139072-131139073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77828024	chr4:131139093-131139094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144903887	chr4:131139117-131139118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572608872	chr4:131139162-131139163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545929610	chr4:131139191-131139192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117894477	chr4:131139194-131139195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs78725538	chr4:131139242-131139243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs70940509	chr4:131139248-131139249	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
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
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Mental retardation	17847001	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Mental retardation	17901693	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:131137400-131138200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:131138800-131139400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:131145600-131146000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:131150400-131151000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:131153400-131154200	Enhancers	Dnd41	blood
6	chr4:131154200-131155400	Flanking Active TSS	Dnd41	blood
7	chr4:131154400-131154600	Active TSS	Liver	Liver
8	chr4:131154400-131155000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr4:131154600-131155000	Flanking Active TSS	Liver	Liver
10	chr4:131154600-131155000	Active TSS	NHLF	lung
11	chr4:131155000-131155200	Enhancers	Liver	Liver
12	chr4:131159400-131159800	Enhancers	HUVEC	blood vessel
13	chr4:131160200-131161600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:131161600-131166600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:131166600-131167800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:131169600-131170400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr4:131169800-131170400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:131169800-131170800	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr4:131170200-131170600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:131172000-131172600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:131172600-131178200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:131177800-131180600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr4:131178200-131179000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr4:131178200-131179000	Enhancers	Muscle Satellite Cultured Cells	--
25	chr4:131178200-131179000	Enhancers	NHDF-Ad	bronchial
26	chr4:131178200-131179200	Enhancers	NHEK	skin
27	chr4:131178200-131179400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr4:131178400-131179000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:131178400-131179000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr4:131178400-131179000	Enhancers	HUVEC	blood vessel
31	chr4:131178400-131179000	Enhancers	NH-A	brain
32	chr4:131178400-131179200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:131178800-131179400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:131178800-131180000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr4:131179000-131179800	Weak transcription	NHDF-Ad	bronchial
36	chr4:131179400-131179800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr4:131179400-131180200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:131179800-131180200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr4:131180000-131180200	Enhancers	NHDF-Ad	bronchial
40	chr4:131187800-131188600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
41	chr4:131191400-131191800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:131191400-131192400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:131191400-131192600	Enhancers	Dnd41	blood
44	chr4:131197600-131198200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr4:131198200-131199200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr4:131199000-131199600	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr4:131199600-131200000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr4:131199800-131200000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr4:131208600-131209400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:131209400-131209800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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