Variant report

Variant	esv3420211
Chromosome Location	chr4:878752-883750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:134)
CpG islands
(count:672)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:134 , 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	chr4:881818-881991	Spleen_OC	spleen:	n/a	n/a
4	CTCF	chr4:881911-881980	Lung_OC	lung:	n/a	n/a
5	CTCF	chr4:881370-881373	GM19239	blood:	n/a	n/a
6	CTCF	chr4:880911-881015	GM19239	blood:	n/a	n/a
7	CTCF	chr4:881254-881363	GM19239	blood:	n/a	n/a
8	CTCF	chr4:881391-881410	GM19239	blood:	n/a	n/a
9	CTCF	chr4:880960-881044	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr4:881416-881526	GM19239	blood:	n/a	n/a
11	HMGN3	chr4:882987-883148	K562	blood:	n/a	n/a
12	HMGN3	chr4:880823-881017	K562	blood:	n/a	n/a
13	MAFF	chr4:878761-878915	HepG2	liver:	n/a	chr4:878848-878866
14	MAFK	chr4:878822-878888	HepG2	liver:	n/a	chr4:878850-878865
15	MAFK	chr4:878848-878885	HepG2	liver:	n/a	chr4:878850-878865
16	MAFK	chr4:879376-879472	HepG2	liver:	n/a	n/a
17	MAFK	chr4:879362-879434	HepG2	liver:	n/a	n/a
18	MAX	chr4:881001-881801	NB4	blood:	n/a	chr4:881556-881566
19	MYC	chr4:881083-881246	MCF-7	breast:	n/a	n/a
20	MYC	chr4:881189-881425	MCF-7	breast:	n/a	n/a
21	MYC	chr4:881170-881177	MCF-7	breast:	n/a	n/a
22	MYC	chr4:881426-881430	MCF-7	breast:	n/a	n/a
23	MYC	chr4:881435-881525	H1-hESC	embryonic stem cell:	n/a	n/a
24	MYC	chr4:881432-881436	MCF-7	breast:	n/a	n/a
25	MYC	chr4:881057-881126	MCF-7	breast:	n/a	n/a
26	NFATC1	chr4:880579-881631	GM12878	blood:	n/a	n/a
27	NFATC1	chr4:880573-881798	GM12878	blood:	n/a	n/a
28	NR2C2	chr4:881107-881768	GM12878	blood:	n/a	n/a
29	PBX3	chr4:880692-881618	GM12878	blood:	n/a	n/a
30	POLR2A	chr4:880785-881061	HUVEC	blood vessel:	n/a	n/a
31	POLR2A	chr4:880494-881208	HepG2	liver:	n/a	n/a
32	POLR2A	chr4:881270-881271	HepG2	liver:	n/a	n/a
33	POLR2A	chr4:879863-880169	GM12878	blood:	n/a	n/a
34	POLR2A	chr4:880239-880289	K562	blood:	n/a	n/a
35	POLR2A	chr4:880635-881826	GM12891	blood:	n/a	n/a
36	POLR2A	chr4:880638-880846	A549	lung:	n/a	n/a
37	POLR2A	chr4:882972-883060	K562	blood:	n/a	n/a
38	POLR2A	chr4:881101-881637	K562	blood:	n/a	n/a
39	POLR2A	chr4:880630-881866	GM12891	blood:	n/a	n/a
40	POLR2A	chr4:880154-880220	GM12878	blood:	n/a	n/a
41	POLR2A	chr4:881382-881432	HepG2	liver:	n/a	n/a
42	POLR2A	chr4:879131-879555	HL-60	blood:	n/a	n/a
43	POLR2A	chr4:882088-882115	K562	blood:	n/a	n/a
44	POLR2A	chr4:880055-880197	K562	blood:	n/a	n/a
45	POLR2A	chr4:880983-881160	A549	lung:	n/a	n/a
46	POLR2A	chr4:880684-881820	GM12878	blood:	n/a	n/a
47	POLR2A	chr4:882217-882254	GM12878	blood:	n/a	n/a
48	POLR2A	chr4:881110-881400	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr4:881162-881598	ProgFib	skin:	n/a	n/a
50	POLR2A	chr4:879162-879513	GM12878	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:881820-881870	Caco-2	colon:	n/a
2	chr4:881820-881870	Caco-2	colon:	n/a
3	chr4:882597-882647	SK-N-SH_RA	brain:	n/a
4	chr4:878727-878777	MCF10A-Er-Src	breast:	n/a
5	chr4:881820-881870	SKMC	muscle:	n/a
6	chr4:881820-881870	ECC-1	luminal epithelium:	n/a
7	chr4:878916-878966	Jurkat	blood:	n/a
8	chr4:881914-881964	BE2_C	brain:	n/a
9	chr4:879432-879482	HepG2	liver:	n/a
10	chr4:882639-882689	HAEpiC	amniotic membrane:	n/a
11	chr4:882639-882689	HepG2	liver:	n/a
12	chr4:878727-878777	ProgFib	skin:	n/a
13	chr4:881914-881964	SKMC	muscle:	n/a
14	chr4:882639-882689	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:882723-882773	RPTEC	kidney:	n/a
16	chr4:882639-882689	Hela-S3	cervix:	n/a
17	chr4:881283-881333	LNCaP	prostate:	n/a
18	chr4:878916-878966	HepG2	liver:	n/a
19	chr4:878916-878966	HRCEpiC	kidney:	n/a
20	chr4:882597-882647	GM19239	blood:	n/a
21	chr4:878916-878966	HRE	kidney:	n/a
22	chr4:879432-879482	PFSK-1	brain:	n/a
23	chr4:882723-882773	GM19239	blood:	n/a
24	chr4:879432-879482	GM12878	blood:	n/a
25	chr4:881914-881964	GM12891	blood:	n/a
26	chr4:881820-881870	K562	blood:	n/a
27	chr4:882639-882689	SK-N-MC	brain:	n/a
28	chr4:882175-882225	AG09309	skin:	n/a
29	chr4:882639-882689	ECC-1	luminal epithelium:	n/a
30	chr4:878727-878777	SK-N-MC	brain:	n/a
31	chr4:878727-878777	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:881283-881333	HCPEpiC	choroid plexus:	n/a
33	chr4:882597-882647	Caco-2	colon:	n/a
34	chr4:878727-878777	NHBE	bronchial:	n/a
35	chr4:879432-879482	ECC-1	luminal epithelium:	n/a
36	chr4:882175-882225	SK-N-SH_RA	brain:	n/a
37	chr4:878810-878860	HAEpiC	amniotic membrane:	n/a
38	chr4:881914-881964	T-47D	breast:	n/a
39	chr4:879432-879482	GM19239	blood:	n/a
40	chr4:878810-878860	IMR90	lung:	fetal
41	chr4:881820-881870	AG04449	skin:	fetal
42	chr4:882723-882773	PFSK-1	brain:	n/a
43	chr4:882723-882773	GM12878	blood:	n/a
44	chr4:882175-882225	PANC-1	pancreas:	n/a
45	chr4:879432-879482	AG09319	gingival:	n/a
46	chr4:879432-879482	NH-A	brain:	n/a
47	chr4:878916-878966	GM12891	blood:	n/a
48	chr4:878810-878860	PrEC	prostate:	n/a
49	chr4:878727-878777	IMR90	lung:	fetal
50	chr4:879432-879482	HEEpiC	esophagus:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:866046..868900-chr4:880612..882674,2	MCF-7	breast:
2	chr4:880176..881824-chr4:882091..883725,2	K562	blood:
3	chr4:880377..884197-chr4:884613..886808,4	K562	blood:
4	chr4:880580..882887-chr4:979285..982250,2	K562	blood:
5	chr4:881197..883636-chr4:883859..886779,2	MCF-7	breast:
6	chr4:868222..869854-chr4:883048..885133,2	MCF-7	breast:
7	chr4:881379..884197-chr4:884613..886808,2	K562	blood:
8	chr4:870064..871608-chr4:881748..883587,2	MCF-7	breast:
9	chr4:880176..881824-chr4:882091..883725,2	K562	blood:
10	chr4:876218..877906-chr4:878500..880701,2	K562	blood:
11	chr4:877520..879506-chr4:881075..883252,2	K562	blood:
12	chr4:876471..879197-chr4:897857..899890,2	K562	blood:
13	chr4:868569..870072-chr4:881118..883830,2	K562	blood:
14	chr4:877520..881136-chr4:881752..884478,3	K562	blood:
15	chr4:876120..878849-chr4:886428..888695,2	K562	blood:

No data

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

Extended variants
information (count: 394 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:394 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186211412	chr4:878753-878754	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs190832535	chr4:878754-878755	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs141203816	chr4:878766-878767	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532274396	chr4:878776-878777	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs543968006	chr4:878778-878779	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs563908519	chr4:878785-878786	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs531087397	chr4:878793-878794	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs549715382	chr4:878802-878803	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs146942840	chr4:878809-878810	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs112078130	chr4:878810-878811	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs557710131	chr4:878812-878813	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs571544342	chr4:878814-878815	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs539172020	chr4:878823-878824	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs147559376	chr4:878833-878834	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs181785635	chr4:878835-878836	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs546165589	chr4:878845-878846	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs564368653	chr4:878847-878848	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs569047883	chr4:878848-878849	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs118070510	chr4:878869-878870	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs6837500	chr4:878871-878872	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs540372533	chr4:878880-878881	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs114745462	chr4:878885-878886	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs138901912	chr4:878892-878893	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs559456962	chr4:878902-878903	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs374626509	chr4:878916-878917	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs6837528	chr4:878917-878918	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs548051969	chr4:878931-878932	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs558569276	chr4:878940-878941	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs186260806	chr4:878959-878960	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs544306301	chr4:878966-878967	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs190333870	chr4:878967-878968	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs149413409	chr4:878976-878977	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs183024840	chr4:878977-878978	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs143752888	chr4:879047-879048	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs187964896	chr4:879062-879063	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs546977689	chr4:879064-879065	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs571620091	chr4:879091-879092	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs191533543	chr4:879092-879093	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs551074916	chr4:879100-879101	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs563219199	chr4:879102-879103	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs574438032	chr4:879127-879128	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs541542529	chr4:879130-879131	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs554384127	chr4:879142-879143	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs566327357	chr4:879145-879146	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs534095665	chr4:879210-879211	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs558530995	chr4:879211-879212	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs576789163	chr4:879239-879240	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs543835786	chr4:879241-879242	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs183067615	chr4:879242-879243	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs574619928	chr4:879250-879251	Weak transcription Strong transcription ZNF genes & repeats 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:262 , 50 per page) page: 1 2 3 4 5 6

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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