Variant report

Variant	esv3421358
Chromosome Location	chr4:939477-942325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:25)
CpG islands
(count:429)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:25 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:939368-939564	HepG2	liver:	n/a	n/a
2	CTCF	chr4:940340-940490	WERI-Rb-1	eye:	n/a	n/a
3	CTCF	chr4:939499-939576	GM20000	blood:	n/a	n/a
4	CTCF	chr4:939380-939530	HBMEC	blood vessel:	n/a	n/a
5	CTCF	chr4:940003-940053	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:940320-940396	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr4:939340-939490	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr4:940284-940313	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr4:939400-939550	HCPEpiC	choroid plexus:	n/a	n/a
10	CTCF	chr4:939493-939496	GM20000	blood:	n/a	n/a
11	EBF1	chr4:940144-940364	GM12878	blood:	n/a	n/a
12	EGR1	chr4:939522-939753	K562	blood:	n/a	n/a
13	FOXP2	chr4:940794-941150	SK-N-MC	brain:	n/a	n/a
14	MAX	chr4:941968-942022	HepG2	liver:	n/a	n/a
15	MYC	chr4:940108-940206	H1-hESC	embryonic stem cell:	n/a	n/a
16	MYC	chr4:940065-940114	MCF-7	breast:	n/a	n/a
17	POLR2A	chr4:941816-941880	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr4:942227-942715	K562	blood:	n/a	n/a
19	POLR2A	chr4:939878-939901	Gliobla	brain:	n/a	n/a
20	RAD21	chr4:939249-939583	H1-hESC	embryonic stem cell:	n/a	chr4:939524-939533
21	RAD21	chr4:939694-939695	A549	lung:	n/a	n/a
22	RAD21	chr4:939408-939608	H1-hESC	embryonic stem cell:	n/a	chr4:939524-939533
23	RAD21	chr4:939498-939569	HepG2	liver:	n/a	chr4:939524-939533
24	RCOR1	chr4:941951-942120	HepG2	liver:	n/a	n/a
25	SIN3A	chr4:939622-939801	H1-hESC	embryonic stem cell:	n/a	chr4:939755-939764

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:940614-940664	AG04450	lung:	fetal
2	chr4:940644-940694	Hepatocyte	liver:	n/a
3	chr4:940614-940664	AG04450	lung:	fetal
4	chr4:940644-940694	Hepatocyte	liver:	n/a
5	chr4:940644-940694	HMEC	breast:	n/a
6	chr4:941966-942016	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:940614-940664	HRCEpiC	kidney:	n/a
8	chr4:940644-940694	GM12891	blood:	n/a
9	chr4:940893-940943	HAEpiC	amniotic membrane:	n/a
10	chr4:942005-942055	NH-A	brain:	n/a
11	chr4:941966-942016	SK-N-SH_RA	brain:	n/a
12	chr4:940644-940694	RPTEC	kidney:	n/a
13	chr4:939597-939647	ProgFib	skin:	n/a
14	chr4:940893-940943	SK-N-SH_RA	brain:	n/a
15	chr4:940614-940664	MCF10A-Er-Src	breast:	n/a
16	chr4:940614-940664	PANC-1	pancreas:	n/a
17	chr4:942005-942055	HNPCEpiC	eye:	n/a
18	chr4:941966-942016	AG04449	skin:	fetal
19	chr4:939597-939647	SAEC	small airway:	n/a
20	chr4:940614-940664	NH-A	brain:	n/a
21	chr4:941054-941104	HRCEpiC	kidney:	n/a
22	chr4:940893-940943	HUVEC	blood vessel:	n/a
23	chr4:941054-941104	A549	lung:	n/a
24	chr4:942005-942055	Hela-S3	cervix:	n/a
25	chr4:940893-940943	BE2_C	brain:	n/a
26	chr4:939597-939647	ovcar-3	ovarian:	n/a
27	chr4:939597-939647	GM12891	blood:	n/a
28	chr4:940893-940943	MCF-7	breast:	n/a
29	chr4:941966-942016	SK-N-SH	brain:	n/a
30	chr4:940614-940664	ovcar-3	ovarian:	n/a
31	chr4:940893-940943	CMK	blood:	n/a
32	chr4:939597-939647	NHBE	bronchial:	n/a
33	chr4:940614-940664	IMR90	lung:	fetal
34	chr4:939597-939647	Caco-2	colon:	n/a
35	chr4:940614-940664	HCT-116	colon:	n/a
36	chr4:942005-942055	HL-60	blood:	n/a
37	chr4:940893-940943	GM12878	blood:	n/a
38	chr4:941054-941104	HCF	heart:	n/a
39	chr4:941054-941104	AG10803	skin:	n/a
40	chr4:940614-940664	SKMC	muscle:	n/a
41	chr4:941054-941104	AG09309	skin:	n/a
42	chr4:940893-940943	HMEC	breast:	n/a
43	chr4:941966-942016	NH-A	brain:	n/a
44	chr4:940644-940694	SK-N-SH_RA	brain:	n/a
45	chr4:941054-941104	HEK293	kidney:	embryo
46	chr4:942005-942055	AG10803	skin:	n/a
47	chr4:939597-939647	HMEC	breast:	n/a
48	chr4:941054-941104	Hela-S3	cervix:	n/a
49	chr4:940893-940943	AoSMC	blood vessel:	n/a
50	chr4:940644-940694	AG09309	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:938534..940525-chr4:942089..943671,2	K562	blood:
2	chr4:925787..928176-chr4:941184..942895,2	MCF-7	breast:
3	chr4:941622..944191-chr4:979532..981778,3	MCF-7	breast:
4	chr4:939199..941933-chr4:945515..948491,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IDUA-3	chr4:939787-939914	NONHSAT094634
2	lnc-IDUA-3	chr4:941497-942377	NONHSAT094632
3	lnc-IDUA-3	chr4:941497-942298	NONHSAT094634
4	lnc-IDUA-3	chr4:941497-941942	NONHSAT094633

No data

Variant related genes	Relation type
TMEM175	TF binding region
TMEM175	CpG island
ENSG00000178950	chromatin interactions
ENSG00000127419	chromatin interactions
ENSG00000145214	chromatin interactions
ENSG00000127415	chromatin interactions

Extended variants
information (count: 167 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:167 , 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	rs560323771	chr4:939488-939489	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs192311513	chr4:939533-939534	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552418384	chr4:939548-939549	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs184867858	chr4:939594-939595	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189700761	chr4:939650-939651	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549585781	chr4:939658-939659	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs567874312	chr4:939673-939674	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs149737452	chr4:939736-939737	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs554033255	chr4:939739-939740	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565569120	chr4:939760-939761	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs113147059	chr4:939768-939769	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs7687129	chr4:939883-939884	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs557754714	chr4:939885-939886	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs371083535	chr4:939907-939908	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs145572387	chr4:939908-939909	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs543493122	chr4:939944-939945	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs556801889	chr4:939946-939947	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574966170	chr4:939986-939987	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs56664216	chr4:940007-940008	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs560816259	chr4:940013-940014	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs572382138	chr4:940052-940053	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs367726970	chr4:940053-940054	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs564110822	chr4:940054-940055	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192665067	chr4:940086-940087	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs74378423	chr4:940097-940098	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs184160438	chr4:940107-940108	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529063851	chr4:940130-940131	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547411316	chr4:940169-940170	Enhancers Genic enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs371562010	chr4:940214-940215	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs113224113	chr4:940222-940223	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs112589666	chr4:940241-940242	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs565982476	chr4:940245-940246	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs188232544	chr4:940302-940303	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs181725879	chr4:940303-940304	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs186305873	chr4:940305-940306	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs537181488	chr4:940319-940320	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs113432984	chr4:940384-940385	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs574959842	chr4:940385-940386	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs536029313	chr4:940391-940392	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs560634720	chr4:940521-940522	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372499273	chr4:940536-940537	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572719254	chr4:940537-940538	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs35560198	chr4:940583-940584	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs77480647	chr4:940601-940602	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs564180320	chr4:940614-940615	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs576026000	chr4:940641-940642	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs546736578	chr4:940645-940646	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs543540204	chr4:940657-940658	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562198324	chr4:940658-940659	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs188911015	chr4:940660-940661	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island Chromatin interactive region	2 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
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Type 2 diabetes	21754918	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:927000-939600	Weak transcription	Spleen	Spleen
2	chr4:927000-940800	Weak transcription	Ovary	ovary
3	chr4:927000-941000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr4:927000-941400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr4:927000-945200	Weak transcription	Colonic Mucosa	Colon
6	chr4:927000-946200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr4:927000-947000	Weak transcription	Aorta	Aorta
8	chr4:927000-948000	Weak transcription	Brain Substantia Nigra	brain
9	chr4:927000-951600	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr4:927000-965800	Weak transcription	HSMMtube	muscle
11	chr4:927200-939800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr4:927200-940400	Weak transcription	Placenta	Placenta
13	chr4:927200-946400	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr4:927200-948600	Weak transcription	Brain Angular Gyrus	brain
15	chr4:927200-952200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr4:927400-940000	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr4:927400-945000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr4:927600-940400	Weak transcription	Stomach Smooth Muscle	stomach
19	chr4:927600-944200	Weak transcription	Primary T cells from cord blood	blood
20	chr4:927600-944400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr4:927600-945200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:927600-955000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:927800-940400	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr4:927800-945200	Weak transcription	Liver	Liver
25	chr4:927800-947200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr4:928000-944600	Weak transcription	Brain Anterior Caudate	brain
27	chr4:928000-945000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr4:928000-945800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr4:928000-946800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr4:928000-947000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:928000-951000	Weak transcription	Rectal Smooth Muscle	rectum
32	chr4:928200-945200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr4:928400-945400	Weak transcription	Brain Hippocampus Middle	brain
34	chr4:928400-945400	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr4:928400-946800	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr4:929000-941000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr4:930000-947400	Weak transcription	Duodenum Mucosa	Duodenum
38	chr4:930800-940400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr4:932000-952400	Weak transcription	Primary B cells from cord blood	blood
40	chr4:933800-965600	Weak transcription	HSMM	muscle
41	chr4:937600-940200	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr4:937800-942400	Weak transcription	Thymus	Thymus
43	chr4:937800-945200	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr4:938000-939800	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr4:938600-942800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr4:938800-939600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr4:938800-940000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
48	chr4:938800-940200	Enhancers	Gastric	stomach
49	chr4:939000-939600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
50	chr4:939000-939600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell

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