Variant report

Variant	nsv4347
Chromosome Location	chr4:57261404-57280595
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:199)
CpG islands
(count:122)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:199 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:57276375-57276720	HepG2	liver:	n/a	n/a
2	ATF2	chr4:57276366-57276850	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:57278823-57278963	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:57278808-57279001	GM12878	blood:	n/a	chr4:57278916-57278927
5	CEBPB	chr4:57276500-57276827	IMR90	lung:	n/a	n/a
6	CEBPB	chr4:57272387-57272708	K562	blood:	n/a	n/a
7	CEBPB	chr4:57276321-57276959	HCT-116	colon:	n/a	n/a
8	CEBPB	chr4:57277435-57277490	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:57263355-57263631	HepG2	liver:	n/a	chr4:57263496-57263507 chr4:57263525-57263536 chr4:57263527-57263538 chr4:57263392-57263405 chr4:57263522-57263539
10	CEBPB	chr4:57272388-57272697	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:57276544-57276748	A549	lung:	n/a	n/a
12	CEBPB	chr4:57272354-57272660	Hela-S3	cervix:	n/a	n/a
13	CHD1	chr4:57277373-57277374	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr4:57276634-57277088	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr4:57275640-57275790	AG04449	skin:	n/a	n/a
16	CTCF	chr4:57263998-57264080	Lung_OC	lung:	n/a	n/a
17	CTCF	chr4:57271500-57271650	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr4:57262790-57262849	GM20000	blood:	n/a	n/a
19	E2F4	chr4:57276434-57276632	MCF10A-Er-Src	breast:	n/a	n/a
20	EP300	chr4:57276319-57276979	ECC-1	luminal epithelium:	n/a	n/a
21	EP300	chr4:57272439-57272543	GM12878	blood:	n/a	n/a
22	EP300	chr4:57276407-57276829	H1-hESC	embryonic stem cell:	n/a	n/a
23	EP300	chr4:57276425-57276754	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr4:57276468-57276776	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr4:57276331-57276726	T-47D	breast:	n/a	n/a
26	EP300	chr4:57266656-57267146	H1-hESC	embryonic stem cell:	n/a	n/a
27	FOS	chr4:57276195-57276903	HUVEC	blood vessel:	n/a	n/a
28	FOS	chr4:57276270-57276876	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr4:57276275-57276842	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr4:57276174-57276853	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr4:57276254-57276865	MCF10A-Er-Src	breast:	n/a	n/a
32	FOSL1	chr4:57276438-57276805	K562	blood:	n/a	n/a
33	FOSL1	chr4:57276302-57277013	HCT-116	colon:	n/a	n/a
34	FOSL1	chr4:57276367-57276974	HCT-116	colon:	n/a	n/a
35	FOSL2	chr4:57276439-57276907	MCF-7	breast:	n/a	n/a
36	FOSL2	chr4:57276433-57276776	A549	lung:	n/a	n/a
37	FOSL2	chr4:57276422-57276873	SK-N-SH	brain:	n/a	n/a
38	FOSL2	chr4:57276487-57276845	HepG2	liver:	n/a	n/a
39	FOXA1	chr4:57276316-57276744	T-47D	breast:	n/a	chr4:57276364-57276376
40	FOXA1	chr4:57276417-57276712	HepG2	liver:	n/a	n/a
41	FOXA1	chr4:57276454-57276736	ECC-1	luminal epithelium:	n/a	n/a
42	FOXA1	chr4:57276334-57276865	HepG2	liver:	n/a	chr4:57276364-57276376
43	FOXA1	chr4:57276373-57276727	ECC-1	luminal epithelium:	n/a	n/a
44	FOXA1	chr4:57276428-57276725	T-47D	breast:	n/a	n/a
45	FOXA1	chr4:57276444-57276826	HepG2	liver:	n/a	n/a
46	FOXA1	chr4:57276455-57276734	HepG2	liver:	n/a	n/a
47	FOXA2	chr4:57276441-57276770	HepG2	liver:	n/a	n/a
48	FOXA2	chr4:57276372-57276989	HepG2	liver:	n/a	n/a
49	FOXA2	chr4:57276484-57276783	A549	lung:	n/a	n/a
50	FOXA2	chr4:57277615-57277975	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:57266977-57267027	IMR90	lung:	fetal
2	chr4:57266977-57267027	AG09309	skin:	n/a
3	chr4:57276595-57276645	ovcar-3	ovarian:	n/a
4	chr4:57266977-57267027	GM12891	blood:	n/a
5	chr4:57276595-57276645	MCF-7	breast:	n/a
6	chr4:57266977-57267027	RPTEC	kidney:	n/a
7	chr4:57266977-57267027	HAEpiC	amniotic membrane:	n/a
8	chr4:57276595-57276645	GM12891	blood:	n/a
9	chr4:57266977-57267027	SKMC	muscle:	n/a
10	chr4:57276595-57276645	AG09319	gingival:	n/a
11	chr4:57266977-57267027	GM12892	blood:	n/a
12	chr4:57266977-57267027	HCPEpiC	choroid plexus:	n/a
13	chr4:57266977-57267027	NHDF-neo	bronchial:	n/a
14	chr4:57276595-57276645	SAEC	small airway:	n/a
15	chr4:57266977-57267027	T-47D	breast:	n/a
16	chr4:57266977-57267027	BJ	skin:	n/a
17	chr4:57276595-57276645	NT2-D1	testis:	n/a
18	chr4:57276595-57276645	BE2_C	brain:	n/a
19	chr4:57276595-57276645	GM19239	blood:	n/a
20	chr4:57266977-57267027	SK-N-SH_RA	brain:	n/a
21	chr4:57276595-57276645	HAEpiC	amniotic membrane:	n/a
22	chr4:57266977-57267027	HEEpiC	esophagus:	n/a
23	chr4:57266977-57267027	HCT-116	colon:	n/a
24	chr4:57266977-57267027	HMEC	breast:	n/a
25	chr4:57276595-57276645	NB4	blood:	n/a
26	chr4:57266977-57267027	NH-A	brain:	n/a
27	chr4:57276595-57276645	PANC-1	pancreas:	n/a
28	chr4:57266977-57267027	SK-N-SH	brain:	n/a
29	chr4:57276595-57276645	ECC-1	luminal epithelium:	n/a
30	chr4:57266977-57267027	Hela-S3	cervix:	n/a
31	chr4:57266977-57267027	HRE	kidney:	n/a
32	chr4:57276595-57276645	SKMC	muscle:	n/a
33	chr4:57276595-57276645	SK-N-SH_RA	brain:	n/a
34	chr4:57276595-57276645	PFSK-1	brain:	n/a
35	chr4:57276595-57276645	T-47D	breast:	n/a
36	chr4:57276595-57276645	GM12892	blood:	n/a
37	chr4:57266977-57267027	PFSK-1	brain:	n/a
38	chr4:57266977-57267027	ovcar-3	ovarian:	n/a
39	chr4:57266977-57267027	AG04449	skin:	fetal
40	chr4:57276595-57276645	HRE	kidney:	n/a
41	chr4:57276595-57276645	GM06990	blood:	n/a
42	chr4:57276595-57276645	NH-A	brain:	n/a
43	chr4:57276595-57276645	HCT-116	colon:	n/a
44	chr4:57266977-57267027	NHBE	bronchial:	n/a
45	chr4:57276595-57276645	SK-N-SH	brain:	n/a
46	chr4:57266977-57267027	MCF10A-Er-Src	breast:	n/a
47	chr4:57276595-57276645	SK-N-MC	brain:	n/a
48	chr4:57266977-57267027	CMK	blood:	n/a
49	chr4:57266977-57267027	ProgFib	skin:	n/a
50	chr4:57276595-57276645	AG09309	skin:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:57261443..57262969-chr4:57269868..57272239,2	K562	blood:
2	chr4:57257925..57261959-chr4:57299598..57302953,3	MCF-7	breast:
3	chr4:57280047..57284869-chr4:57288459..57291870,6	K562	blood:
4	chr4:57252177..57255146-chr4:57278604..57280682,2	MCF-7	breast:
5	chr4:57279724..57281835-chr4:57300459..57302841,3	MCF-7	breast:
6	chr4:57269980..57272538-chr4:57276339..57278488,2	K562	blood:
7	chr4:57252113..57256281-chr4:57265528..57268374,5	MCF-7	breast:
8	chr1:150551501..150552089-chr4:57266112..57266895,2	NB4	blood:
9	chr4:57275711..57277429-chr4:57298915..57301727,2	K562	blood:
10	chr4:57273341..57278355-chr4:57278652..57283436,7	K562	blood:
11	chr4:57275040..57277242-chr4:57300118..57301937,2	MCF-7	breast:
12	chr4:57277811..57280010-chr4:57300306..57302094,2	MCF-7	breast:
13	chr4:57252303..57254207-chr4:57266105..57268233,2	MCF-7	breast:
14	chr4:57265375..57267060-chr4:57284878..57287823,2	K562	blood:
15	chr4:57265970..57269312-chr4:57270989..57273638,4	MCF-7	breast:
16	chr4:57268824..57271246-chr4:57301014..57303212,2	K562	blood:
17	chr4:57278722..57280888-chr4:57296778..57299271,2	MCF-7	breast:
18	chr4:57265142..57270324-chr4:57301712..57304176,5	K562	blood:
19	chr4:57273341..57277197-chr4:57279767..57282535,3	K562	blood:
20	chr4:57274956..57277925-chr4:57332751..57335099,2	MCF-7	breast:
21	chr4:57256994..57259922-chr4:57269239..57271312,2	K562	blood:
22	chr4:57268050..57270580-chr4:57305183..57307241,2	K562	blood:
23	chr4:57256866..57258507-chr4:57276793..57279015,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAICS-2	chr4:57262478-57263037	ENSG00000270147.1

No data

Variant related genes	Relation type
PPAT	TF binding region
ENSG00000268171	TF binding region
ENSG00000270147	TF binding region
PPAT	CpG island
ENSG00000268171	CpG island
ENSG00000270147	CpG island
ENSG00000268171	chromatin interactions
ENSG00000269921	chromatin interactions
ENSG00000128059	chromatin interactions
ENSG00000157426	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000174780	chromatin interactions
ENSG00000128050	chromatin interactions
ENSG00000270147	chromatin interactions

Extended variants
information (count: 678 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186916603	chr4:57261408-57261409	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs113509123	chr4:57261449-57261450	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs200268394	chr4:57261524-57261525	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs371980582	chr4:57261527-57261528	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs144451574	chr4:57261568-57261569	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs375085596	chr4:57261605-57261606	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs2660744	chr4:57261610-57261611	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs147822472	chr4:57261646-57261647	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs3908150	chr4:57261652-57261653	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs76674380	chr4:57261656-57261657	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs2412738	chr4:57261665-57261666	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs527367886	chr4:57261679-57261680	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs560199458	chr4:57261713-57261714	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs375102221	chr4:57261717-57261718	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201443229	chr4:57261729-57261730	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs371829709	chr4:57261744-57261745	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs562778842	chr4:57261771-57261772	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs531437922	chr4:57261772-57261773	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs148674920	chr4:57261783-57261784	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs191710770	chr4:57261788-57261789	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs530139363	chr4:57261798-57261799	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs564877775	chr4:57261800-57261801	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs76917475	chr4:57261838-57261839	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs34716907	chr4:57261841-57261842	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs397878327	chr4:57261842-57261843	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs200655048	chr4:57261854-57261855	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs527387459	chr4:57261866-57261867	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547054681	chr4:57261875-57261876	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs551842725	chr4:57261882-57261883	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs566794520	chr4:57261955-57261956	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs539021955	chr4:57262046-57262047	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs552623017	chr4:57262083-57262084	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs569518963	chr4:57262122-57262123	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs369465909	chr4:57262223-57262224	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs372126151	chr4:57262303-57262304	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs113759324	chr4:57262404-57262405	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs555204119	chr4:57262454-57262455	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs568627913	chr4:57262460-57262461	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs141632507	chr4:57262486-57262487	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs372708166	chr4:57262488-57262489	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs146221614	chr4:57262546-57262547	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs576790641	chr4:57262580-57262581	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs564078504	chr4:57262590-57262591	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs545765378	chr4:57262638-57262639	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs566943962	chr4:57262647-57262648	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs183766324	chr4:57262724-57262725	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs373657410	chr4:57262732-57262733	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs541677937	chr4:57262745-57262746	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs201250405	chr4:57262758-57262759	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs376043196	chr4:57262775-57262776	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Breast cancer	21785460	CNVD
Medullary thyroid carcinoma	18765511	CNVD

Chromatin state (count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:57254200-57273800	Weak transcription	Spleen	Spleen
2	chr4:57254400-57268400	Weak transcription	Lung	lung
3	chr4:57254400-57273600	Weak transcription	Pancreas	Pancrea
4	chr4:57254600-57264000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:57254600-57271600	Weak transcription	Ovary	ovary
6	chr4:57254600-57276400	Weak transcription	Psoas Muscle	Psoas
7	chr4:57254600-57280200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr4:57254800-57261800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr4:57254800-57262000	Weak transcription	Placenta	Placenta
10	chr4:57254800-57264000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr4:57254800-57264000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr4:57254800-57271600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr4:57254800-57273200	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr4:57254800-57275200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr4:57254800-57275400	Weak transcription	Rectal Smooth Muscle	rectum
16	chr4:57254800-57276400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr4:57254800-57276400	Weak transcription	Right Ventricle	heart
18	chr4:57254800-57276600	Weak transcription	Left Ventricle	heart
19	chr4:57254800-57287600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr4:57255000-57262200	Weak transcription	A549	lung
21	chr4:57255000-57264400	Weak transcription	Brain Germinal Matrix	brain
22	chr4:57255000-57264800	Weak transcription	Primary B cells from peripheral blood	blood
23	chr4:57255000-57265600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr4:57255000-57266000	Weak transcription	Primary B cells from cord blood	blood
25	chr4:57255000-57266200	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr4:57255000-57266200	Weak transcription	NH-A	brain
27	chr4:57255000-57266400	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr4:57255000-57266400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr4:57255000-57266600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr4:57255000-57266600	Weak transcription	HSMM	muscle
31	chr4:57255000-57266800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr4:57255000-57269200	Weak transcription	Fetal Muscle Trunk	muscle
33	chr4:57255000-57271400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr4:57255200-57262000	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr4:57255200-57262200	Weak transcription	Fetal Lung	lung
36	chr4:57255200-57262200	Weak transcription	Osteobl	bone
37	chr4:57255200-57264000	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr4:57255200-57264000	Weak transcription	Fetal Stomach	stomach
39	chr4:57255200-57266200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:57255200-57266200	Weak transcription	HUVEC	blood vessel
41	chr4:57255200-57266400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr4:57255200-57266800	Weak transcription	Fetal Kidney	kidney
43	chr4:57255200-57266800	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr4:57255200-57267200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr4:57255200-57267400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr4:57255200-57271600	Weak transcription	NHEK	skin
47	chr4:57255200-57272200	Weak transcription	Stomach Smooth Muscle	stomach
48	chr4:57255200-57275600	Weak transcription	NHLF	lung
49	chr4:57255200-57276400	Weak transcription	Colon Smooth Muscle	Colon
50	chr4:57255200-57276600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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