Variant report

Variant	esv3436386
Chromosome Location	chr4:920377-922925
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:920257-920608	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr4:922125-922477	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:920532-920533	K562	blood:	n/a	n/a
4	CTCF	chr4:920400-920550	HPAF	blood vessel:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
5	CTCF	chr4:920440-920590	SAEC	small airway:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
6	CTCF	chr4:920460-920610	HA-sp	spinal cord:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
7	CTCF	chr4:920480-920630	NHEK	skin:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
8	CTCF	chr4:920400-920550	AG10803	skin:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
9	CTCF	chr4:920500-920650	HFF-Myc	foreskin:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
10	CTCF	chr4:920400-920550	GM06990	blood:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
11	CTCF	chr4:920400-920550	WI-38	lung:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
12	CTCF	chr4:920480-920630	HVMF	connective:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
13	CTCF	chr4:920420-920570	HMF	breast:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
14	CTCF	chr4:920400-920550	HAc	cerebellar:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
15	CTCF	chr4:920420-920570	AG04450	lung:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
16	CTCF	chr4:920460-920610	HCFaa	heart:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
17	CTCF	chr4:920261-920660	A549	lung:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
18	CTCF	chr4:920440-920590	HVMF	connective:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
19	CTCF	chr4:920320-920470	HA-sp	spinal cord:	n/a	n/a
20	CTCF	chr4:920380-920530	GM12873	blood:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
21	CTCF	chr4:920500-920650	HCM	heart:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
22	CTCF	chr4:920460-920610	SAEC	small airway:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
23	CTCF	chr4:920400-920550	AG04450	lung:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
24	CTCF	chr4:920420-920570	HRE	kidney:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
25	CTCF	chr4:920360-920510	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr4:920440-920590	K562	blood:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
27	CTCF	chr4:920338-920571	HepG2	liver:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
28	CTCF	chr4:920440-920590	HUVEC	blood vessel:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
29	CTCF	chr4:920460-920610	AoAF	blood vessel:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
30	CTCF	chr4:920400-920550	RPTEC	kidney:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
31	CTCF	chr4:920239-920659	MCF-7	breast:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
32	CTCF	chr4:920440-920590	HepG2	liver:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
33	CTCF	chr4:920440-920590	HMF	breast:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
34	CTCF	chr4:920460-920610	HUVEC	blood vessel:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
35	CTCF	chr4:920480-920630	NHDF-neo	bronchial:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
36	CTCF	chr4:920460-920610	GM12864	blood:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
37	CTCF	chr4:920418-920618	MCF-7	breast:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
38	CTCF	chr4:920440-920590	A549	lung:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
39	CTCF	chr4:920374-920630	K562	blood:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
40	CTCF	chr4:920380-920530	GM12872	blood:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
41	CTCF	chr4:920296-920630	H1-hESC	embryonic stem cell:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
42	CTCF	chr4:920466-920556	Spleen_OC	spleen:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
43	CTCF	chr4:920387-920629	A549	lung:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
44	CTCF	chr4:920313-920560	A549	lung:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
45	CTCF	chr4:920440-920590	BJ	skin:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
46	CTCF	chr4:920371-920627	GM12878	blood:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
47	CTCF	chr4:920400-920550	HEEpiC	esophagus:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
48	CTCF	chr4:920460-920610	K562	blood:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
49	CTCF	chr4:920440-920590	HCPEpiC	choroid plexus:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521
50	CTCF	chr4:920320-920653	K562	blood:	n/a	chr4:920509-920527 chr4:920512-920525 chr4:920512-920521

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:921637-921687	HAEpiC	amniotic membrane:	n/a
2	chr4:920607-920657	IMR90	lung:	fetal
3	chr4:920971-921021	NHDF-neo	bronchial:	n/a
4	chr4:921295-921345	MCF10A-Er-Src	breast:	n/a
5	chr4:920971-921021	SK-N-SH	brain:	n/a
6	chr4:920971-921021	GM12878	blood:	n/a
7	chr4:921637-921687	GM06990	blood:	n/a
8	chr4:921295-921345	HepG2	liver:	n/a
9	chr4:921637-921687	PFSK-1	brain:	n/a
10	chr4:920607-920657	LNCaP	prostate:	n/a
11	chr4:921295-921345	HIPEpiC	eye:	n/a
12	chr4:920607-920657	CMK	blood:	n/a
13	chr4:921295-921345	A549	lung:	n/a
14	chr4:920971-921021	AoSMC	blood vessel:	n/a
15	chr4:920971-921021	AG09319	gingival:	n/a
16	chr4:920607-920657	PrEC	prostate:	n/a
17	chr4:921295-921345	HCPEpiC	choroid plexus:	n/a
18	chr4:921637-921687	SKMC	muscle:	n/a
19	chr4:921637-921687	ProgFib	skin:	n/a
20	chr4:921637-921687	T-47D	breast:	n/a
21	chr4:921637-921687	ECC-1	luminal epithelium:	n/a
22	chr4:920971-921021	NB4	blood:	n/a
23	chr4:920607-920657	GM19239	blood:	n/a
24	chr4:920971-921021	GM12891	blood:	n/a
25	chr4:921295-921345	NT2-D1	testis:	n/a
26	chr4:921295-921345	AG04450	lung:	fetal
27	chr4:921295-921345	NHDF-neo	bronchial:	n/a
28	chr4:920607-920657	HEEpiC	esophagus:	n/a
29	chr4:921295-921345	HMEC	breast:	n/a
30	chr4:920607-920657	HNPCEpiC	eye:	n/a
31	chr4:921637-921687	HepG2	liver:	n/a
32	chr4:920971-921021	T-47D	breast:	n/a
33	chr4:921637-921687	AG09309	skin:	n/a
34	chr4:920971-921021	PFSK-1	brain:	n/a
35	chr4:920607-920657	HPAEpiC	pulmonary alveolar:	n/a
36	chr4:921295-921345	MCF-7	breast:	n/a
37	chr4:921295-921345	HAEpiC	amniotic membrane:	n/a
38	chr4:920971-921021	BE2_C	brain:	n/a
39	chr4:921637-921687	HL-60	blood:	n/a
40	chr4:921295-921345	SAEC	small airway:	n/a
41	chr4:920971-921021	CMK	blood:	n/a
42	chr4:920971-921021	Hepatocyte	liver:	n/a
43	chr4:921295-921345	HEK293	kidney:	embryo
44	chr4:921637-921687	HCPEpiC	choroid plexus:	n/a
45	chr4:921295-921345	AoSMC	blood vessel:	n/a
46	chr4:920607-920657	K562	blood:	n/a
47	chr4:921637-921687	NHBE	bronchial:	n/a
48	chr4:921295-921345	GM06990	blood:	n/a
49	chr4:920971-921021	SK-N-MC	brain:	n/a
50	chr4:921637-921687	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:910127..911959-chr4:919976..922093,2	K562	blood:
2	chr4:920431..925400-chr4:1002690..1006792,6	K562	blood:
3	chr4:922193..925879-chr4:967045..969349,3	MCF-7	breast:
4	chr4:773213..775149-chr4:920055..922373,2	K562	blood:
5	chr4:904418..909522-chr4:918936..921597,4	K562	blood:
6	chr4:900673..902303-chr4:918486..920857,2	K562	blood:
7	chr4:899878..903573-chr4:921540..925410,3	K562	blood:
8	chr4:922716..929032-chr4:963622..968729,9	MCF-7	breast:
9	chr4:920442..922045-chr4:924333..926135,2	MCF-7	breast:
10	chr4:919599..922522-chr4:986652..989402,2	K562	blood:
11	chr4:920273..922423-chr4:994508..996161,2	K562	blood:

Variant related genes	Relation type
TMEM175	TF binding region
TMEM175	CpG island
ENSG00000178950	chromatin interactions
ENSG00000145214	chromatin interactions
ENSG00000127418	chromatin interactions
ENSG00000145217	chromatin interactions

Extended variants
information (count: 164 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:164 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543317286	chr4:920382-920383	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs539753760	chr4:920383-920384	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs561882232	chr4:920384-920385	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs188775495	chr4:920388-920389	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs35042719	chr4:920393-920394	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs112388755	chr4:920395-920396	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs559479169	chr4:920411-920412	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs527933548	chr4:920432-920433	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs552780693	chr4:920452-920453	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs571193726	chr4:920472-920473	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs532069279	chr4:920475-920476	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs550163518	chr4:920495-920496	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs557750971	chr4:920507-920508	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs550169936	chr4:920516-920517	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs56353809	chr4:920526-920527	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs180830586	chr4:920572-920573	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs554290705	chr4:920578-920579	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs565815411	chr4:920605-920606	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs1249903	chr4:920612-920613	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs55987370	chr4:920634-920635	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs1249902	chr4:920649-920650	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs112408943	chr4:920659-920660	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs113187740	chr4:920663-920664	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs113304040	chr4:920667-920668	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs185829278	chr4:920672-920673	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs555426407	chr4:920680-920681	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs113076184	chr4:920702-920703	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs7376683	chr4:920705-920706	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs539282704	chr4:920712-920713	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs376440633	chr4:920721-920722	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs191124125	chr4:920725-920726	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs112209047	chr4:920729-920730	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs111656492	chr4:920737-920738	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs562745992	chr4:920779-920780	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs7375353	chr4:920787-920788	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs151261048	chr4:920795-920796	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs560088750	chr4:920803-920804	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs527665750	chr4:920813-920814	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs549147362	chr4:920824-920825	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs7375358	chr4:920835-920836	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs7376701	chr4:920836-920837	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs377734807	chr4:920858-920859	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs201580176	chr4:920861-920862	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs113656777	chr4:920868-920869	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs181933151	chr4:920877-920878	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs373347583	chr4:920887-920888	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs531713601	chr4:920898-920899	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs80150671	chr4:920909-920910	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs79625599	chr4:920910-920911	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs200970728	chr4:920915-920916	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Breast cancer	22522925	CNVD
Type 2 diabetes	21754918	CNVD

Chromatin state (count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:897000-924800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:905400-922200	Weak transcription	HepG2	liver
3	chr4:905600-923000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr4:906800-924000	Weak transcription	NHLF	lung
5	chr4:906800-924800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr4:907000-924600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr4:907200-923200	Weak transcription	Brain Angular Gyrus	brain
8	chr4:907200-924200	Weak transcription	Fetal Brain Female	brain
9	chr4:907400-923800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:907600-923800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr4:907600-924000	Weak transcription	Brain Germinal Matrix	brain
12	chr4:907600-924000	Weak transcription	Fetal Muscle Leg	muscle
13	chr4:909200-922800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:909200-923000	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr4:909400-924600	Weak transcription	Rectal Smooth Muscle	rectum
16	chr4:909600-923200	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr4:910800-925200	Weak transcription	Aorta	Aorta
18	chr4:913800-921600	Weak transcription	Psoas Muscle	Psoas
19	chr4:915000-920600	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr4:915400-920600	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr4:915400-920600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr4:915800-924000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr4:916000-924000	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr4:916000-924600	Weak transcription	Brain Substantia Nigra	brain
25	chr4:916800-924000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:917000-920400	Enhancers	Primary B cells from cord blood	blood
27	chr4:917000-921600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr4:917000-922800	Weak transcription	Dnd41	blood
29	chr4:917000-924200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr4:917200-922200	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr4:917200-924000	Weak transcription	Fetal Thymus	thymus
32	chr4:917200-924600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr4:917800-920600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr4:918000-920400	Enhancers	K562	blood
35	chr4:918000-920600	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr4:918000-920600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr4:918400-920400	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr4:918400-920400	Enhancers	Adipose Nuclei	Adipose
39	chr4:918400-920600	Enhancers	Stomach Mucosa	stomach
40	chr4:918400-923800	Weak transcription	HSMM	muscle
41	chr4:918600-920400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr4:918600-920400	Enhancers	GM12878-XiMat	blood
43	chr4:918600-920600	Enhancers	Right Ventricle	heart
44	chr4:918600-921600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr4:918600-923800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr4:918800-923600	Weak transcription	Osteobl	bone
47	chr4:918800-924800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr4:919000-920600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr4:919000-920600	Enhancers	Left Ventricle	heart
50	chr4:919000-920600	Genic enhancers	Lung	lung

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