Variant report

Variant	nsv10414
Chromosome Location	chr4:696527-701955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:413)
CpG islands
(count:733)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:696568-696761	K562	blood:	n/a	n/a
2	BHLHE40	chr4:699146-699836	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:699601-699851	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:696406-696678	K562	blood:	n/a	n/a
5	BHLHE40	chr4:699172-699754	K562	blood:	n/a	n/a
6	BRCA1	chr4:699246-699395	HepG2	liver:	n/a	n/a
7	BRCA1	chr4:699438-699725	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr4:696629-696699	HepG2	liver:	n/a	n/a
9	CBX3	chr4:698708-699492	K562	blood:	n/a	n/a
10	CCNT2	chr4:698263-698583	K562	blood:	n/a	n/a
11	CCNT2	chr4:699219-699986	K562	blood:	n/a	n/a
12	CCNT2	chr4:696425-696732	K562	blood:	n/a	n/a
13	CEBPB	chr4:698750-699349	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr4:696515-696687	K562	blood:	n/a	n/a
15	CEBPD	chr4:699428-699895	HepG2	liver:	n/a	n/a
16	CHD1	chr4:698766-700226	IMR90	lung:	n/a	n/a
17	CHD1	chr4:699022-699031	GM12878	blood:	n/a	n/a
18	CHD2	chr4:699252-699802	GM12878	blood:	n/a	n/a
19	CHD2	chr4:699649-699755	K562	blood:	n/a	n/a
20	CHD2	chr4:699024-699441	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr4:699130-699449	K562	blood:	n/a	n/a
22	CHD2	chr4:696445-696782	K562	blood:	n/a	n/a
23	CHD2	chr4:699122-699862	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr4:699329-699341	HepG2	liver:	n/a	n/a
25	CREB1	chr4:699493-699883	A549	lung:	n/a	n/a
26	CREB1	chr4:699211-699489	A549	lung:	n/a	n/a
27	CTCF	chr4:699339-699430	GM19239	blood:	n/a	n/a
28	CTCF	chr4:699678-699781	K562	blood:	n/a	n/a
29	CTCF	chr4:699350-699496	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr4:700374-700398	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr4:699298-699359	GM12891	blood:	n/a	n/a
32	CTCF	chr4:699530-699649	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr4:700425-700439	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr4:699517-699520	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr4:699336-699337	GM19239	blood:	n/a	n/a
36	CUX1	chr4:698883-698886	K562	blood:	n/a	n/a
37	E2F4	chr4:699256-699657	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F6	chr4:699293-699550	K562	blood:	n/a	n/a
39	E2F6	chr4:699620-699950	K562	blood:	n/a	n/a
40	E2F6	chr4:696458-696643	K562	blood:	n/a	n/a
41	E2F6	chr4:696364-696956	K562	blood:	n/a	n/a
42	E2F6	chr4:699178-699874	K562	blood:	n/a	n/a
43	E2F6	chr4:699226-699595	K562	blood:	n/a	n/a
44	E2F6	chr4:699300-699616	A549	lung:	n/a	n/a
45	E2F6	chr4:699143-699600	A549	lung:	n/a	n/a
46	EBF1	chr4:701018-701912	GM12878	blood:	n/a	chr4:701263-701274
47	EBF1	chr4:701005-701920	GM12878	blood:	n/a	chr4:701263-701274
48	EBF1	chr4:701031-701583	GM12878	blood:	n/a	chr4:701263-701274
49	EGR1	chr4:699420-699627	GM12878	blood:	n/a	chr4:699521-699535
50	EGR1	chr4:699344-699725	K562	blood:	n/a	chr4:699521-699535

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:699224-699274	MCF-7	breast:	n/a
2	chr4:699224-699274	MCF-7	breast:	n/a
3	chr4:699950-700000	SK-N-SH	brain:	n/a
4	chr4:698616-698666	BE2_C	brain:	n/a
5	chr4:698303-698353	HCT-116	colon:	n/a
6	chr4:699224-699274	PANC-1	pancreas:	n/a
7	chr4:699691-699741	AoSMC	blood vessel:	n/a
8	chr4:699372-699422	AG10803	skin:	n/a
9	chr4:700219-700269	GM12892	blood:	n/a
10	chr4:699691-699741	ECC-1	luminal epithelium:	n/a
11	chr4:698616-698666	SKMC	muscle:	n/a
12	chr4:698616-698666	SK-N-SH	brain:	n/a
13	chr4:700219-700269	NB4	blood:	n/a
14	chr4:698303-698353	AG09319	gingival:	n/a
15	chr4:698303-698353	PFSK-1	brain:	n/a
16	chr4:699288-699338	Caco-2	colon:	n/a
17	chr4:699224-699274	SK-N-MC	brain:	n/a
18	chr4:698303-698353	NH-A	brain:	n/a
19	chr4:699691-699741	HCT-116	colon:	n/a
20	chr4:699372-699422	HCT-116	colon:	n/a
21	chr4:699386-699436	GM12891	blood:	n/a
22	chr4:699691-699741	HNPCEpiC	eye:	n/a
23	chr4:699435-699485	GM06990	blood:	n/a
24	chr4:698616-698666	Jurkat	blood:	n/a
25	chr4:698480-698530	Jurkat	blood:	n/a
26	chr4:699435-699485	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:699288-699338	HEEpiC	esophagus:	n/a
28	chr4:699224-699274	SK-N-SH	brain:	n/a
29	chr4:698616-698666	ProgFib	skin:	n/a
30	chr4:699386-699436	NHDF-neo	bronchial:	n/a
31	chr4:699386-699436	GM06990	blood:	n/a
32	chr4:700219-700269	HAEpiC	amniotic membrane:	n/a
33	chr4:700219-700269	ProgFib	skin:	n/a
34	chr4:699386-699436	HUVEC	blood vessel:	n/a
35	chr4:699372-699422	NH-A	brain:	n/a
36	chr4:699401-699451	SK-N-MC	brain:	n/a
37	chr4:699950-700000	GM12892	blood:	n/a
38	chr4:699386-699436	HepG2	liver:	n/a
39	chr4:699372-699422	CMK	blood:	n/a
40	chr4:699372-699422	HCM	heart:	n/a
41	chr4:699224-699274	ovcar-3	ovarian:	n/a
42	chr4:699950-700000	NH-A	brain:	n/a
43	chr4:699691-699741	AG04450	lung:	fetal
44	chr4:699950-700000	CMK	blood:	n/a
45	chr4:699401-699451	ProgFib	skin:	n/a
46	chr4:699950-700000	Jurkat	blood:	n/a
47	chr4:699691-699741	HRCEpiC	kidney:	n/a
48	chr4:699386-699436	AG10803	skin:	n/a
49	chr4:699691-699741	GM19239	blood:	n/a
50	chr4:699372-699422	GM06990	blood:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:672428..678608-chr4:693605..699154,7	MCF-7	breast:
2	chr4:680242..683670-chr4:697022..701034,8	MCF-7	breast:
3	chr4:666647..668169-chr4:694233..696531,2	K562	blood:
4	chr4:681693..683683-chr4:698278..699853,2	K562	blood:
5	chr4:701224..703407-chr4:720806..724106,3	K562	blood:
6	chr4:666011..668174-chr4:698640..701171,3	K562	blood:
7	chr4:691381..694386-chr4:695506..698892,4	K562	blood:
8	chr4:681383..683193-chr4:698223..700658,3	K562	blood:
9	chr4:698332..701237-chr4:701746..703364,2	K562	blood:
10	chr4:696628..698929-chr4:713327..715075,2	MCF-7	breast:
11	chr4:674123..676409-chr4:700716..703557,3	K562	blood:
12	chr4:701349..702978-chr4:774069..776105,2	MCF-7	breast:
13	chr4:666295..671517-chr4:698228..703248,8	MCF-7	breast:
14	chr4:700678..704217-chr4:710705..714201,3	MCF-7	breast:
15	chr4:694824..697589-chr4:697861..699485,2	K562	blood:
16	chr4:674123..675815-chr4:701035..703606,2	K562	blood:
17	chr4:666625..669025-chr4:694883..696562,2	MCF-7	breast:
18	chr4:699605..701232-chr4:847515..849852,2	K562	blood:
19	chr4:684700..687240-chr4:700658..702428,2	MCF-7	breast:
20	chr4:694824..697589-chr4:697861..699485,2	K562	blood:
21	chr4:673793..676751-chr4:694911..696578,2	K562	blood:
22	chr4:679478..681319-chr4:699446..701129,2	K562	blood:
23	chr4:679574..681875-chr4:700268..702006,2	K562	blood:
24	chr4:697549..703820-chr4:770860..775722,9	K562	blood:
25	chr4:673479..675144-chr4:696764..699498,2	K562	blood:
26	chr4:693450..697481-chr4:699717..703370,4	K562	blood:
27	chr4:682326..684833-chr4:700614..702994,2	MCF-7	breast:
28	chr4:700770..703438-chr4:730148..732108,2	K562	blood:
29	chr4:683107..685849-chr4:694318..697240,2	K562	blood:
30	chr4:693289..694985-chr4:696803..698794,2	MCF-7	breast:
31	chr4:672883..676399-chr4:697081..701106,5	MCF-7	breast:
32	chr17:73773135..73777353-chr4:698527..702357,3	MCF-7	breast:
33	chr4:701950..703734-chr4:716320..717930,2	K562	blood:
34	chr4:701026..702736-chr4:705955..708606,2	K562	blood:
35	chr4:666292..671732-chr4:694079..701503,8	MCF-7	breast:

No data

Variant related genes	Relation type
PCGF3	TF binding region
PCGF3	CpG island
ENSG00000215375	chromatin interactions
ENSG00000185619	chromatin interactions
ENSG00000169020	chromatin interactions
ENSG00000248416	chromatin interactions
ENSG00000249592	chromatin interactions
ENSG00000169026	chromatin interactions
ENSG00000178950	chromatin interactions
ENSG00000132475	chromatin interactions

Extended variants
information (count: 327 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:327 , 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	rs550054184	chr4:696532-696533	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs373369092	chr4:696539-696540	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs567938970	chr4:696603-696604	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs528901647	chr4:696616-696617	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs547151804	chr4:696617-696618	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs58167498	chr4:696644-696645	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs534380435	chr4:696651-696652	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs559152442	chr4:696688-696689	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs533608861	chr4:696701-696702	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs538509377	chr4:696708-696709	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs376716369	chr4:696720-696721	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs182301578	chr4:696800-696801	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs12646225	chr4:696848-696849	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs187083751	chr4:696859-696860	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs374469188	chr4:696886-696887	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs573429191	chr4:696891-696892	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs544398772	chr4:696929-696930	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs563136974	chr4:696945-696946	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs572247476	chr4:697100-697101	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs545903700	chr4:697131-697132	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs563893201	chr4:697133-697134	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs561708262	chr4:697171-697172	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs28547545	chr4:697196-697197	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs143611510	chr4:697214-697215	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs562040363	chr4:697276-697277	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs528877052	chr4:697284-697285	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs547408248	chr4:697297-697298	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs386670421	chr4:697303-697304	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs375531118	chr4:697304-697305	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs371109969	chr4:697308-697309	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs191096302	chr4:697367-697368	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs182896075	chr4:697368-697369	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs28379067	chr4:697371-697372	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs568783185	chr4:697372-697373	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs112224574	chr4:697390-697391	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs367825747	chr4:697429-697430	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs535473268	chr4:697439-697440	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs370383243	chr4:697446-697447	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs34593579	chr4:697461-697462	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs527700757	chr4:697481-697482	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs55969231	chr4:697488-697489	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs549428703	chr4:697493-697494	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs564448354	chr4:697507-697508	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs79739589	chr4:697604-697605	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs138081769	chr4:697607-697608	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs76057807	chr4:697615-697616	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs142570333	chr4:697630-697631	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs561822117	chr4:697667-697668	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs35590636	chr4:697697-697698	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs569037627	chr4:697702-697703	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:679 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:683600-697200	Weak transcription	Gastric	stomach
2	chr4:683600-699000	Weak transcription	Right Atrium	heart
3	chr4:684200-699000	Weak transcription	Right Ventricle	heart
4	chr4:687400-697800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr4:693400-698800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr4:693600-698000	Weak transcription	Esophagus	oesophagus
7	chr4:693600-698800	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr4:693600-698800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr4:693600-698800	Weak transcription	Hela-S3	cervix
10	chr4:693800-698600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr4:693800-698800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr4:693800-698800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr4:693800-698800	Weak transcription	Liver	Liver
14	chr4:694000-698200	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr4:694000-698800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:694000-698800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:694000-698800	Weak transcription	Primary B cells from cord blood	blood
18	chr4:694000-698800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr4:694000-698800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:694000-698800	Weak transcription	Fetal Thymus	thymus
21	chr4:694000-698800	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr4:694000-699000	Weak transcription	GM12878-XiMat	blood
23	chr4:694200-696600	Weak transcription	NHEK	skin
24	chr4:694200-698400	Weak transcription	Colonic Mucosa	Colon
25	chr4:694200-698800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:694200-699000	Weak transcription	Primary hematopoietic stem cells	blood
27	chr4:694400-698600	Weak transcription	Primary B cells from peripheral blood	blood
28	chr4:694400-698600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr4:694600-698600	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr4:694600-698800	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr4:694800-697200	Weak transcription	Spleen	Spleen
32	chr4:694800-698800	Weak transcription	Duodenum Mucosa	Duodenum
33	chr4:694800-699000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr4:695000-697600	Weak transcription	Placenta	Placenta
35	chr4:695000-698600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr4:695000-699000	Weak transcription	Brain Angular Gyrus	brain
37	chr4:696000-699000	Enhancers	Stomach Mucosa	stomach
38	chr4:696200-697000	Enhancers	Fetal Intestine Small	intestine
39	chr4:696200-697000	Flanking Active TSS	K562	blood
40	chr4:696400-697000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:696400-697000	Enhancers	Fetal Intestine Large	intestine
42	chr4:696600-697000	Enhancers	NHEK	skin
43	chr4:696800-697600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:697000-697200	Enhancers	Brain Anterior Caudate	brain
45	chr4:697000-697800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr4:697000-698800	Weak transcription	NHEK	skin
47	chr4:697000-699000	Weak transcription	Fetal Intestine Large	intestine
48	chr4:697000-699000	Enhancers	K562	blood
49	chr4:697200-697400	Enhancers	Brain Hippocampus Middle	brain
50	chr4:697200-697400	Enhancers	Gastric	stomach

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