Variant report

Variant	esv3418584
Chromosome Location	chr4:879252-882850
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:120)
CpG islands
(count:489)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:120 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr4:880639-881818	GM12878	blood:	n/a	n/a
2	BCL3	chr4:880567-881666	GM12878	blood:	n/a	n/a
3	CTCF	chr4:881254-881363	GM19239	blood:	n/a	n/a
4	CTCF	chr4:881370-881373	GM19239	blood:	n/a	n/a
5	CTCF	chr4:881416-881526	GM19239	blood:	n/a	n/a
6	CTCF	chr4:880911-881015	GM19239	blood:	n/a	n/a
7	CTCF	chr4:880960-881044	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr4:881391-881410	GM19239	blood:	n/a	n/a
9	CTCF	chr4:881911-881980	Lung_OC	lung:	n/a	n/a
10	CTCF	chr4:881818-881991	Spleen_OC	spleen:	n/a	n/a
11	HMGN3	chr4:880823-881017	K562	blood:	n/a	n/a
12	MAFK	chr4:879362-879434	HepG2	liver:	n/a	n/a
13	MAFK	chr4:879376-879472	HepG2	liver:	n/a	n/a
14	MAX	chr4:881001-881801	NB4	blood:	n/a	chr4:881556-881566
15	MYC	chr4:881426-881430	MCF-7	breast:	n/a	n/a
16	MYC	chr4:881170-881177	MCF-7	breast:	n/a	n/a
17	MYC	chr4:881435-881525	H1-hESC	embryonic stem cell:	n/a	n/a
18	MYC	chr4:881083-881246	MCF-7	breast:	n/a	n/a
19	MYC	chr4:881189-881425	MCF-7	breast:	n/a	n/a
20	MYC	chr4:881057-881126	MCF-7	breast:	n/a	n/a
21	MYC	chr4:881432-881436	MCF-7	breast:	n/a	n/a
22	NFATC1	chr4:880579-881631	GM12878	blood:	n/a	n/a
23	NFATC1	chr4:880573-881798	GM12878	blood:	n/a	n/a
24	NR2C2	chr4:881107-881768	GM12878	blood:	n/a	n/a
25	PBX3	chr4:880692-881618	GM12878	blood:	n/a	n/a
26	POLR2A	chr4:880555-881962	GM12878	blood:	n/a	n/a
27	POLR2A	chr4:880641-881741	GM12891	blood:	n/a	n/a
28	POLR2A	chr4:882027-884795	K562	blood:	n/a	n/a
29	POLR2A	chr4:879863-880169	GM12878	blood:	n/a	n/a
30	POLR2A	chr4:880702-881847	GM12878	blood:	n/a	n/a
31	POLR2A	chr4:880927-881532	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr4:881101-881637	K562	blood:	n/a	n/a
33	POLR2A	chr4:879811-880235	K562	blood:	n/a	n/a
34	POLR2A	chr4:881096-881103	A549	lung:	n/a	n/a
35	POLR2A	chr4:881043-881245	K562	blood:	n/a	n/a
36	POLR2A	chr4:882708-883141	GM12878	blood:	n/a	n/a
37	POLR2A	chr4:881295-881569	MCF-7	breast:	n/a	n/a
38	POLR2A	chr4:880873-880993	A549	lung:	n/a	n/a
39	POLR2A	chr4:881445-881475	GM12878	blood:	n/a	n/a
40	POLR2A	chr4:879190-879355	GM12878	blood:	n/a	n/a
41	POLR2A	chr4:880630-881866	GM12891	blood:	n/a	n/a
42	POLR2A	chr4:880469-881927	GM12892	blood:	n/a	n/a
43	POLR2A	chr4:882314-883208	GM12878	blood:	n/a	n/a
44	POLR2A	chr4:880635-881826	GM12891	blood:	n/a	n/a
45	POLR2A	chr4:881885-882125	GM12878	blood:	n/a	n/a
46	POLR2A	chr4:879152-879476	K562	blood:	n/a	n/a
47	POLR2A	chr4:880785-881061	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr4:881285-881460	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr4:879131-879555	HL-60	blood:	n/a	n/a
50	POLR2A	chr4:881049-881051	A549	lung:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:882175-882225	HRCEpiC	kidney:	n/a
2	chr4:882175-882225	HRCEpiC	kidney:	n/a
3	chr4:881914-881964	AoSMC	blood vessel:	n/a
4	chr4:881283-881333	NH-A	brain:	n/a
5	chr4:882597-882647	AG10803	skin:	n/a
6	chr4:881283-881333	NB4	blood:	n/a
7	chr4:882639-882689	AG04450	lung:	fetal
8	chr4:882723-882773	GM12891	blood:	n/a
9	chr4:879432-879482	HAEpiC	amniotic membrane:	n/a
10	chr4:882723-882773	BJ	skin:	n/a
11	chr4:879432-879482	HEK293	kidney:	embryo
12	chr4:882723-882773	HMEC	breast:	n/a
13	chr4:879432-879482	K562	blood:	n/a
14	chr4:882639-882689	IMR90	lung:	fetal
15	chr4:881283-881333	SK-N-SH	brain:	n/a
16	chr4:881914-881964	GM12878	blood:	n/a
17	chr4:881283-881333	HNPCEpiC	eye:	n/a
18	chr4:879432-879482	Jurkat	blood:	n/a
19	chr4:881283-881333	Hepatocyte	liver:	n/a
20	chr4:881914-881964	Hela-S3	cervix:	n/a
21	chr4:882639-882689	HRE	kidney:	n/a
22	chr4:882723-882773	HCT-116	colon:	n/a
23	chr4:879432-879482	NHDF-neo	bronchial:	n/a
24	chr4:881914-881964	AG09319	gingival:	n/a
25	chr4:881820-881870	AG04450	lung:	fetal
26	chr4:882639-882689	BJ	skin:	n/a
27	chr4:881820-881870	SK-N-SH_RA	brain:	n/a
28	chr4:881914-881964	HRPEpiC	eye:	n/a
29	chr4:881914-881964	HCPEpiC	choroid plexus:	n/a
30	chr4:882723-882773	HRCEpiC	kidney:	n/a
31	chr4:881820-881870	HMEC	breast:	n/a
32	chr4:882639-882689	PANC-1	pancreas:	n/a
33	chr4:882639-882689	ProgFib	skin:	n/a
34	chr4:881283-881333	T-47D	breast:	n/a
35	chr4:881914-881964	ovcar-3	ovarian:	n/a
36	chr4:881914-881964	IMR90	lung:	fetal
37	chr4:882723-882773	PFSK-1	brain:	n/a
38	chr4:881820-881870	Hela-S3	cervix:	n/a
39	chr4:881914-881964	HUVEC	blood vessel:	n/a
40	chr4:882175-882225	H1-hESC	embryonic stem cell:	embryo
41	chr4:881283-881333	SAEC	small airway:	n/a
42	chr4:881914-881964	SKMC	muscle:	n/a
43	chr4:882723-882773	SK-N-SH	brain:	n/a
44	chr4:882597-882647	GM06990	blood:	n/a
45	chr4:879432-879482	A549	lung:	n/a
46	chr4:882723-882773	MCF-7	breast:	n/a
47	chr4:882175-882225	CMK	blood:	n/a
48	chr4:882597-882647	ECC-1	luminal epithelium:	n/a
49	chr4:881820-881870	MCF-7	breast:	n/a
50	chr4:881820-881870	HRE	kidney:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:881379..884197-chr4:884613..886808,2	K562	blood:
2	chr4:880176..881824-chr4:882091..883725,2	K562	blood:
3	chr4:880176..881824-chr4:882091..883725,2	K562	blood:
4	chr4:877520..881136-chr4:881752..884478,3	K562	blood:
5	chr4:876218..877906-chr4:878500..880701,2	K562	blood:
6	chr4:868569..870072-chr4:881118..883830,2	K562	blood:
7	chr4:877520..879506-chr4:881075..883252,2	K562	blood:
8	chr4:870064..871608-chr4:881748..883587,2	MCF-7	breast:
9	chr4:881197..883636-chr4:883859..886779,2	MCF-7	breast:
10	chr4:880377..884197-chr4:884613..886808,4	K562	blood:
11	chr4:866046..868900-chr4:880612..882674,2	MCF-7	breast:
12	chr4:880580..882887-chr4:979285..982250,2	K562	blood:

No data

Variant related genes	Relation type
GAK	TF binding region
GAK	CpG island
ENSG00000178950	chromatin interactions
ENSG00000127415	chromatin interactions
ENSG00000145214	chromatin interactions

Extended variants
information (count: 301 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541939832	chr4:879255-879256	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs561515857	chr4:879262-879263	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs530747592	chr4:879263-879264	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs187760562	chr4:879269-879270	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs540935226	chr4:879282-879283	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs114257072	chr4:879296-879297	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs138369476	chr4:879311-879312	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs550730301	chr4:879324-879325	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs142845413	chr4:879352-879353	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs375141916	chr4:879384-879385	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs530179452	chr4:879451-879452	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs548229342	chr4:879456-879457	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs117524401	chr4:879477-879478	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs533714958	chr4:879513-879514	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs568797900	chr4:879514-879515	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs75131424	chr4:879515-879516	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs562757394	chr4:879519-879520	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs538128462	chr4:879521-879522	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs372299695	chr4:879530-879531	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs113111576	chr4:879551-879552	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs376680256	chr4:879563-879564	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs11933491	chr4:879570-879571	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs556236975	chr4:879599-879600	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs574485045	chr4:879684-879685	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs146062754	chr4:879735-879736	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs76033377	chr4:879753-879754	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs35003788	chr4:879769-879770	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs573403993	chr4:879773-879774	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs28662837	chr4:879776-879777	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs565458213	chr4:879806-879807	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs577505456	chr4:879813-879814	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs192336977	chr4:879832-879833	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs184760730	chr4:879839-879840	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs529995718	chr4:879840-879841	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs548291112	chr4:879896-879897	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs564398475	chr4:879912-879913	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs527765346	chr4:879913-879914	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs62297079	chr4:879977-879978	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs570616480	chr4:879984-879985	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs141799007	chr4:879987-879988	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs550057063	chr4:879992-879993	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs377503069	chr4:880017-880018	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs535409442	chr4:880022-880023	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs17781378	chr4:880094-880095	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs565669957	chr4:880114-880115	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs539508202	chr4:880115-880116	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs558931399	chr4:880119-880120	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs79748657	chr4:880155-880156	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs74775400	chr4:880174-880175	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs113490505	chr4:880207-880208	Weak transcription Strong transcription Genic enhancers	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:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:841200-881200	Strong transcription	Brain Germinal Matrix	brain
2	chr4:841200-881200	Strong transcription	Duodenum Mucosa	Duodenum
3	chr4:841200-898600	Strong transcription	Cortex derived primary cultured neurospheres	brain
4	chr4:841200-898800	Strong transcription	Placenta	Placenta
5	chr4:841200-901400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr4:841200-906000	Strong transcription	Stomach Smooth Muscle	stomach
7	chr4:841400-884400	Strong transcription	Brain Hippocampus Middle	brain
8	chr4:841400-892000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:841400-907400	Strong transcription	Sigmoid Colon	Sigmoid Colon
10	chr4:842000-881200	Strong transcription	Lung	lung
11	chr4:842000-907400	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr4:842200-907600	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr4:844200-907600	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr4:847200-920000	Weak transcription	Right Atrium	heart
15	chr4:848200-884600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr4:849800-885000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr4:849800-892200	Strong transcription	Colonic Mucosa	Colon
18	chr4:850200-884200	Strong transcription	Duodenum Smooth Muscle	Duodenum
19	chr4:850200-892000	Strong transcription	Primary B cells from peripheral blood	blood
20	chr4:850400-896200	Strong transcription	Skeletal Muscle Female	skeletal muscle
21	chr4:850600-892400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:853400-891000	Weak transcription	Stomach Mucosa	stomach
23	chr4:853800-899400	Strong transcription	Dnd41	blood
24	chr4:856800-895600	Strong transcription	Fetal Brain Female	brain
25	chr4:857200-900200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:857400-884600	Strong transcription	Liver	Liver
27	chr4:857400-885400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr4:857400-899200	Strong transcription	Fetal Intestine Small	intestine
29	chr4:857400-906000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr4:857400-909600	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr4:858000-907400	Strong transcription	Fetal Stomach	stomach
32	chr4:858200-884400	Strong transcription	Aorta	Aorta
33	chr4:861200-881200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:861200-881400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr4:861400-881800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr4:861600-899200	Strong transcription	Fetal Intestine Large	intestine
37	chr4:861800-907400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:862000-880800	Strong transcription	Placenta Amnion	Placenta Amnion
39	chr4:863000-881600	Strong transcription	Spleen	Spleen
40	chr4:863400-881000	Strong transcription	Esophagus	oesophagus
41	chr4:863800-880000	Strong transcription	NHLF	lung
42	chr4:863800-880200	Strong transcription	Right Ventricle	heart
43	chr4:863800-881200	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr4:863800-881200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:864000-880600	Strong transcription	Pancreas	Pancrea
46	chr4:864000-881000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr4:864000-881000	Strong transcription	Gastric	stomach
48	chr4:864000-881200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr4:864000-881200	Weak transcription	Fetal Kidney	kidney
50	chr4:864000-881400	Weak transcription	Hela-S3	cervix

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