Variant report

Variant	esv3398607
Chromosome Location	chr4:861452-865050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:126)
CpG islands
(count:429)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:126 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr4:863428-864091	GM12878	blood:	n/a	n/a
2	BCL3	chr4:863395-864132	GM12878	blood:	n/a	n/a
3	BCL3	chr4:862730-862996	GM12878	blood:	n/a	n/a
4	CTCF	chr4:862905-862925	GM13976	blood:	n/a	n/a
5	CTCF	chr4:862797-863256	GM19239	blood:	n/a	n/a
6	CTCF	chr4:863531-863535	GM13976	blood:	n/a	n/a
7	CTCF	chr4:863467-863529	GM13976	blood:	n/a	n/a
8	CTCF	chr4:863793-863908	GM12891	blood:	n/a	n/a
9	CTCF	chr4:863407-863442	GM19239	blood:	n/a	n/a
10	CTCF	chr4:863739-863789	GM12891	blood:	n/a	n/a
11	CTCF	chr4:863478-863904	GM19239	blood:	n/a	n/a
12	CTCF	chr4:862840-862990	GM12872	blood:	n/a	n/a
13	CTCF	chr4:862963-862969	GM12892	blood:	n/a	n/a
14	FOSL2	chr4:862817-863549	HepG2	liver:	n/a	n/a
15	HMGN3	chr4:862173-862380	K562	blood:	n/a	n/a
16	HMGN3	chr4:861515-861643	K562	blood:	n/a	n/a
17	IRF4	chr4:863125-863622	GM12878	blood:	n/a	n/a
18	MAFF	chr4:863189-863256	HepG2	liver:	n/a	n/a
19	MAFK	chr4:863135-863198	IMR90	lung:	n/a	n/a
20	MAFK	chr4:863087-863263	HepG2	liver:	n/a	n/a
21	MXI1	chr4:863690-863926	HepG2	liver:	n/a	n/a
22	MYC	chr4:863491-863523	MCF-7	breast:	n/a	n/a
23	MYC	chr4:863554-863570	MCF-7	breast:	n/a	n/a
24	MYC	chr4:862968-863033	HUVEC	blood vessel:	n/a	n/a
25	MYC	chr4:863597-863666	GM12878	blood:	n/a	n/a
26	MYC	chr4:863071-863159	GM12878	blood:	n/a	n/a
27	MYC	chr4:863650-863724	MCF-7	breast:	n/a	n/a
28	NFATC1	chr4:863434-864134	GM12878	blood:	n/a	n/a
29	NFATC1	chr4:863393-864113	GM12878	blood:	n/a	n/a
30	NFIC	chr4:863546-863973	GM12878	blood:	n/a	n/a
31	NR2C2	chr4:862712-863919	GM12878	blood:	n/a	n/a
32	PAX5	chr4:862985-863729	GM12878	blood:	n/a	n/a
33	PAX5	chr4:863202-863669	GM12878	blood:	n/a	n/a
34	PAX5	chr4:863073-863549	GM12878	blood:	n/a	n/a
35	PAX5	chr4:863287-863459	GM12878	blood:	n/a	n/a
36	PBX3	chr4:862863-863190	GM12878	blood:	n/a	n/a
37	PBX3	chr4:863199-864029	GM12878	blood:	n/a	n/a
38	POLR2A	chr4:864132-864188	HepG2	liver:	n/a	n/a
39	POLR2A	chr4:863453-864578	K562	blood:	n/a	n/a
40	POLR2A	chr4:862606-863982	GM12878	blood:	n/a	n/a
41	POLR2A	chr4:863383-863472	K562	blood:	n/a	n/a
42	POLR2A	chr4:863016-863018	MCF-7	breast:	n/a	n/a
43	POLR2A	chr4:863734-863764	MCF-7	breast:	n/a	n/a
44	POLR2A	chr4:862411-862839	K562	blood:	n/a	n/a
45	POLR2A	chr4:862977-863606	GM12891	blood:	n/a	n/a
46	POLR2A	chr4:862843-863015	HepG2	liver:	n/a	n/a
47	POLR2A	chr4:862909-863323	K562	blood:	n/a	n/a
48	POLR2A	chr4:862569-864172	GM12892	blood:	n/a	n/a
49	POLR2A	chr4:863741-863841	GM12878	blood:	n/a	n/a
50	POLR2A	chr4:861659-861725	HepG2	liver:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:864597-864647	BE2_C	brain:	n/a
2	chr4:864100-864150	ECC-1	luminal epithelium:	n/a
3	chr4:864597-864647	BE2_C	brain:	n/a
4	chr4:864100-864150	ECC-1	luminal epithelium:	n/a
5	chr4:864840-864890	Hela-S3	cervix:	n/a
6	chr4:864017-864067	HAEpiC	amniotic membrane:	n/a
7	chr4:863878-863928	HRCEpiC	kidney:	n/a
8	chr4:864995-865045	HIPEpiC	eye:	n/a
9	chr4:864840-864890	AoSMC	blood vessel:	n/a
10	chr4:864017-864067	HCM	heart:	n/a
11	chr4:864995-865045	SK-N-SH	brain:	n/a
12	chr4:863878-863928	AG04449	skin:	fetal
13	chr4:864597-864647	HMEC	breast:	n/a
14	chr4:862561-862611	PFSK-1	brain:	n/a
15	chr4:864100-864150	PANC-1	pancreas:	n/a
16	chr4:864597-864647	PrEC	prostate:	n/a
17	chr4:863878-863928	LNCaP	prostate:	n/a
18	chr4:864017-864067	MCF10A-Er-Src	breast:	n/a
19	chr4:864017-864067	ovcar-3	ovarian:	n/a
20	chr4:864100-864150	AG09319	gingival:	n/a
21	chr4:863878-863928	HNPCEpiC	eye:	n/a
22	chr4:864017-864067	AG09309	skin:	n/a
23	chr4:863878-863928	IMR90	lung:	fetal
24	chr4:863878-863928	MCF10A-Er-Src	breast:	n/a
25	chr4:863878-863928	Hela-S3	cervix:	n/a
26	chr4:862561-862611	AG09319	gingival:	n/a
27	chr4:864100-864150	AG04450	lung:	fetal
28	chr4:864995-865045	ovcar-3	ovarian:	n/a
29	chr4:864100-864150	SKMC	muscle:	n/a
30	chr4:864017-864067	SK-N-SH_RA	brain:	n/a
31	chr4:863878-863928	U87	brain:	n/a
32	chr4:864597-864647	GM12878	blood:	n/a
33	chr4:864840-864890	A549	lung:	n/a
34	chr4:864100-864150	HAEpiC	amniotic membrane:	n/a
35	chr4:863878-863928	SK-N-SH	brain:	n/a
36	chr4:863878-863928	MCF-7	breast:	n/a
37	chr4:864100-864150	LNCaP	prostate:	n/a
38	chr4:864100-864150	CMK	blood:	n/a
39	chr4:862561-862611	HMEC	breast:	n/a
40	chr4:862561-862611	SAEC	small airway:	n/a
41	chr4:864017-864067	HCF	heart:	n/a
42	chr4:864995-865045	HCT-116	colon:	n/a
43	chr4:864840-864890	HCT-116	colon:	n/a
44	chr4:864597-864647	IMR90	lung:	fetal
45	chr4:864597-864647	RPTEC	kidney:	n/a
46	chr4:864017-864067	MCF-7	breast:	n/a
47	chr4:864017-864067	GM12878	blood:	n/a
48	chr4:864840-864890	HCPEpiC	choroid plexus:	n/a
49	chr4:864017-864067	AoSMC	blood vessel:	n/a
50	chr4:864840-864890	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:860816..863391-chr4:864528..866341,2	K562	blood:

No data

Variant related genes	Relation type
GAK	TF binding region
GAK	CpG island
ENSG00000178950	chromatin interactions

Extended variants
information (count: 223 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:223 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540588813	chr4:861456-861457	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs565385427	chr4:861481-861482	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs73207789	chr4:861497-861498	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs3733352	chr4:861498-861499	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs144757449	chr4:861499-861500	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs529822817	chr4:861522-861523	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs376101685	chr4:861558-861559	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs562231076	chr4:861570-861571	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs560010552	chr4:861594-861595	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs375776415	chr4:861617-861618	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs180809473	chr4:861623-861624	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs3733351	chr4:861628-861629	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs537571188	chr4:861630-861631	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs549832503	chr4:861639-861640	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs3822026	chr4:861652-861653	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs376890285	chr4:861799-861800	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569553599	chr4:861814-861815	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs536838200	chr4:861848-861849	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs11947128	chr4:861880-861881	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs138629594	chr4:861887-861888	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs186095991	chr4:861893-861894	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs150470486	chr4:861931-861932	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs56986122	chr4:861936-861937	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs577144349	chr4:861946-861947	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs544412363	chr4:861948-861949	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs556611256	chr4:861971-861972	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs6854553	chr4:861998-861999	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs541576274	chr4:862041-862042	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs569312919	chr4:862051-862052	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs534634403	chr4:862054-862055	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs191095270	chr4:862101-862102	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs2306245	chr4:862156-862157	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs562726965	chr4:862161-862162	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs563960569	chr4:862187-862188	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs531330568	chr4:862199-862200	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs549659721	chr4:862204-862205	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs568117430	chr4:862245-862246	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs35802687	chr4:862257-862258	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs181798150	chr4:862291-862292	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs114673114	chr4:862307-862308	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs536905414	chr4:862310-862311	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs377645498	chr4:862318-862319	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs115244803	chr4:862340-862341	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs371808360	chr4:862341-862342	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs147004796	chr4:862342-862343	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs535238444	chr4:862353-862354	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs375149692	chr4:862354-862355	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs112202640	chr4:862361-862362	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs34585705	chr4:862363-862364	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs79029749	chr4:862364-862365	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:841200-862600	Strong transcription	Esophagus	oesophagus
2	chr4:841200-872800	Strong transcription	Rectal Mucosa Donor 29	rectum
3	chr4:841200-881200	Strong transcription	Brain Germinal Matrix	brain
4	chr4:841200-881200	Strong transcription	Duodenum Mucosa	Duodenum
5	chr4:841200-898600	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr4:841200-898800	Strong transcription	Placenta	Placenta
7	chr4:841200-901400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:841200-906000	Strong transcription	Stomach Smooth Muscle	stomach
9	chr4:841400-870800	Strong transcription	Primary T cells from cord blood	blood
10	chr4:841400-884400	Strong transcription	Brain Hippocampus Middle	brain
11	chr4:841400-892000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:841400-907400	Strong transcription	Sigmoid Colon	Sigmoid Colon
13	chr4:841600-864000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr4:842000-881200	Strong transcription	Lung	lung
15	chr4:842000-907400	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr4:842200-907600	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr4:843200-863600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr4:844200-866400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr4:844200-907600	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr4:844600-864600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr4:846800-864800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:847200-920000	Weak transcription	Right Atrium	heart
23	chr4:848200-884600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:848400-862800	Strong transcription	NHLF	lung
25	chr4:848400-863000	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr4:848600-862600	Strong transcription	Brain Angular Gyrus	brain
27	chr4:849400-863000	Strong transcription	Right Ventricle	heart
28	chr4:849600-864800	Strong transcription	Brain Substantia Nigra	brain
29	chr4:849800-875400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr4:849800-885000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr4:849800-892200	Strong transcription	Colonic Mucosa	Colon
32	chr4:850000-864800	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr4:850000-878200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
34	chr4:850200-866400	Strong transcription	Adipose Nuclei	Adipose
35	chr4:850200-871400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr4:850200-872400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr4:850200-884200	Strong transcription	Duodenum Smooth Muscle	Duodenum
38	chr4:850200-892000	Strong transcription	Primary B cells from peripheral blood	blood
39	chr4:850400-862600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:850400-862600	Strong transcription	Gastric	stomach
41	chr4:850400-862800	Strong transcription	Skeletal Muscle Male	skeletal muscle
42	chr4:850400-864400	Strong transcription	Rectal Smooth Muscle	rectum
43	chr4:850400-864600	Strong transcription	Muscle Satellite Cultured Cells	--
44	chr4:850400-868400	Strong transcription	Brain Cingulate Gyrus	brain
45	chr4:850400-896200	Strong transcription	Skeletal Muscle Female	skeletal muscle
46	chr4:850600-870800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr4:850600-871400	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr4:850600-892400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:850800-872000	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr4:850800-872400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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