Variant report

Variant	nsv1000447
Chromosome Location	chr4:78191608-78291173
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	ARID3A	chr4:78268651-78268718	HepG2	liver:	n/a	n/a
2	ATF1	chr4:78267547-78267723	K562	blood:	n/a	n/a
3	BHLHE40	chr4:78265976-78266449	GM12878	blood:	n/a	n/a
4	BRCA1	chr4:78230084-78230356	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr4:78263269-78263765	HCT-116	colon:	n/a	n/a
6	CBX3	chr4:78263352-78263680	HCT-116	colon:	n/a	n/a
7	CBX3	chr4:78253746-78254319	HCT-116	colon:	n/a	n/a
8	CBX3	chr4:78253883-78254139	K562	blood:	n/a	n/a
9	CBX3	chr4:78263330-78263629	K562	blood:	n/a	n/a
10	CBX3	chr4:78253824-78254202	K562	blood:	n/a	n/a
11	CEBPB	chr4:78268366-78268440	K562	blood:	n/a	chr4:78268368-78268377 chr4:78268366-78268379 chr4:78268368-78268379
12	CEBPB	chr4:78215392-78215580	K562	blood:	n/a	chr4:78215544-78215555
13	CEBPB	chr4:78226915-78227276	MCF-7	breast:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
14	CEBPB	chr4:78268359-78268485	IMR90	lung:	n/a	chr4:78268368-78268377 chr4:78268366-78268379 chr4:78268368-78268379
15	CEBPB	chr4:78226987-78227290	HepG2	liver:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
16	CEBPB	chr4:78215423-78215638	IMR90	lung:	n/a	chr4:78215544-78215555
17	CEBPB	chr4:78215400-78215689	HepG2	liver:	n/a	chr4:78215544-78215555
18	CEBPB	chr4:78227010-78227248	Hela-S3	cervix:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
19	CEBPB	chr4:78268252-78268595	HepG2	liver:	n/a	chr4:78268368-78268377 chr4:78268366-78268379 chr4:78268368-78268379
20	CEBPB	chr4:78226971-78227260	K562	blood:	n/a	chr4:78227117-78227130 chr4:78227117-78227128 chr4:78227118-78227129 chr4:78227117-78227130
21	CHD2	chr4:78254095-78254505	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr4:78230108-78230195	HepG2	liver:	n/a	n/a
23	CTCF	chr4:78288035-78288417	A549	lung:	n/a	chr4:78288200-78288218 chr4:78288203-78288216 chr4:78288202-78288223
24	CTCF	chr4:78230118-78230284	GM20000	blood:	n/a	n/a
25	CTCF	chr4:78279580-78279730	AG04450	lung:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
26	CTCF	chr4:78230060-78230210	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr4:78279580-78279730	GM12873	blood:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
28	CTCF	chr4:78288320-78288470	NHEK	skin:	n/a	n/a
29	CTCF	chr4:78230120-78230270	HL-60	blood:	n/a	n/a
30	CTCF	chr4:78253184-78253229	LNCaP	prostate:	n/a	n/a
31	CTCF	chr4:78275280-78275430	GM12871	blood:	n/a	n/a
32	CTCF	chr4:78230100-78230336	Gliobla	brain:	n/a	n/a
33	CTCF	chr4:78279560-78279710	GM06990	blood:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
34	CTCF	chr4:78274927-78275274	MCF-7	breast:	n/a	chr4:78275103-78275121 chr4:78275105-78275126 chr4:78275106-78275119
35	CTCF	chr4:78206420-78206570	HPF	lung:	n/a	n/a
36	CTCF	chr4:78288063-78288358	K562	blood:	n/a	chr4:78288200-78288218 chr4:78288203-78288216 chr4:78288202-78288223
37	CTCF	chr4:78281040-78281190	AG10803	skin:	n/a	n/a
38	CTCF	chr4:78229940-78230090	HRE	kidney:	n/a	n/a
39	CTCF	chr4:78279620-78279770	NB4	blood:	n/a	chr4:78279670-78279686 chr4:78279664-78279685 chr4:78279676-78279683 chr4:78279671-78279684 chr4:78279669-78279687
40	CTCF	chr4:78230120-78230270	HPF	lung:	n/a	n/a
41	CTCF	chr4:78274840-78274990	HMF	breast:	n/a	n/a
42	CTCF	chr4:78288340-78288490	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr4:78288053-78288376	GM13977	blood:	n/a	chr4:78288200-78288218 chr4:78288203-78288216 chr4:78288202-78288223
44	CTCF	chr4:78288082-78288328	Kidney_OC	kidney:	n/a	chr4:78288200-78288218 chr4:78288203-78288216 chr4:78288202-78288223
45	CTCF	chr4:78275200-78275350	GM12872	blood:	n/a	n/a
46	CTCF	chr4:78274948-78275275	ProgFib	skin:	n/a	chr4:78275103-78275121 chr4:78275105-78275126 chr4:78275106-78275119
47	CTCF	chr4:78227000-78227150	HMF	breast:	n/a	chr4:78227096-78227117 chr4:78227101-78227119 chr4:78227103-78227116
48	CTCF	chr4:78275240-78275390	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr4:78274957-78275275	MCF-7	breast:	n/a	chr4:78275103-78275121 chr4:78275105-78275126 chr4:78275106-78275119
50	CTCF	chr4:78280080-78280230	AG04449	skin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:78278110..78280443-chr4:78281438..78283101,2	MCF-7	breast:
2	chr4:78161188..78162532-chr4:78229476..78230856,15	MCF-7	breast:
3	chr4:78257188..78259774-chr4:78266144..78268332,2	K562	blood:
4	chr4:78289830..78292754-chr4:78299148..78300754,2	K562	blood:
5	chr4:78161416..78162110-chr4:78226527..78227315,3	MCF-7	breast:
6	chr4:78155252..78157365-chr4:78224145..78227144,3	MCF-7	breast:
7	chr4:78160754..78162321-chr4:78226906..78228617,2	MCF-7	breast:
8	chr4:78174499..78176837-chr4:78205161..78207032,2	MCF-7	breast:
9	chr4:78287913..78288436-chr4:78619834..78620825,2	MCF-7	breast:
10	chr4:78161365..78162334-chr4:78279195..78280134,7	K562	blood:
11	chr4:78287359..78291622-chr4:78351702..78357008,5	MCF-7	breast:
12	chr4:78161311..78162711-chr4:78226629..78227614,14	MCF-7	breast:
13	chr4:78236163..78238480-chr4:78287943..78289669,2	K562	blood:
14	chr4:78257188..78259774-chr4:78266144..78268332,2	K562	blood:
15	chr4:78161398..78162211-chr4:78229720..78230660,3	MCF-7	breast:
16	chr4:78266632..78268344-chr4:78268869..78271315,2	K562	blood:
17	chr4:78230184..78230702-chr4:78278364..78278865,2	MCF-7	breast:
18	chr4:77973179..77974099-chr4:78229775..78230650,3	K562	blood:
19	chr4:78278110..78280443-chr4:78281438..78283101,2	MCF-7	breast:
20	chr4:78236163..78238480-chr4:78287943..78289669,2	K562	blood:
21	chr4:78266632..78268344-chr4:78268869..78271315,2	K562	blood:
22	chr4:78161721..78162270-chr4:78279119..78279681,2	MCF-7	breast:
23	chr4:78158067..78160012-chr4:78227264..78228770,2	MCF-7	breast:
24	chr4:78162165..78163774-chr4:78227168..78228953,2	MCF-7	breast:
25	chr4:78270382..78272050-chr4:78274178..78276131,2	K562	blood:
26	chr4:78229797..78230625-chr4:78279333..78280102,3	MCF-7	breast:
27	chr4:78161284..78162458-chr4:78229777..78230742,7	K562	blood:
28	chr4:78161324..78162321-chr4:78279149..78280134,4	MCF-7	breast:
29	chr4:78287667..78288571-chr4:78353781..78354626,3	MCF-7	breast:
30	chr4:78229797..78230625-chr4:78279333..78280102,3	MCF-7	breast:
31	chr4:78230184..78230702-chr4:78278364..78278865,2	MCF-7	breast:
32	chr4:78270382..78272050-chr4:78274178..78276131,2	K562	blood:
33	chr4:78269918..78271823-chr4:78272380..78274841,2	MCF-7	breast:
34	chr1:118958475..118959178-chr4:78279470..78280113,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNI-5	chr4:78232550-78233264	NONHSAT097052
2	lnc-CCNI-6	chr4:78271523-78272388	NONHSAT097053

Variant related genes	Relation type
ENSG00000248831	TF binding region
ENSG00000250006	TF binding region
ENSG00000248831	chromatin interactions

Extended variants
information (count: 4989 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4989 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543725907	chr4:78191640-78191641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs137935880	chr4:78191643-78191644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574106822	chr4:78191658-78191659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542823364	chr4:78191669-78191670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114899729	chr4:78191713-78191714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115567961	chr4:78191730-78191731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4330372	chr4:78191776-78191777	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs563958687	chr4:78191815-78191816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4476627	chr4:78191820-78191821	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs4464596	chr4:78191830-78191831	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs188802520	chr4:78191836-78191837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111783378	chr4:78191846-78191847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549236244	chr4:78191928-78191929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186068901	chr4:78191964-78191965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373829487	chr4:78191992-78191993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189365985	chr4:78191999-78192000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533494128	chr4:78192032-78192033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146164802	chr4:78192075-78192076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537459465	chr4:78192083-78192084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs17395298	chr4:78192172-78192173	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs114905562	chr4:78192190-78192191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542809365	chr4:78192208-78192209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182566696	chr4:78192219-78192220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140127009	chr4:78192256-78192257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115770377	chr4:78192282-78192283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564228134	chr4:78192295-78192296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142144630	chr4:78192305-78192306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10491463	chr4:78192318-78192319	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs568559641	chr4:78192343-78192344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563423484	chr4:78192376-78192377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185945278	chr4:78192393-78192394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191140646	chr4:78192408-78192409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146321013	chr4:78192409-78192410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534836615	chr4:78192450-78192451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557191030	chr4:78192461-78192462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551541463	chr4:78192463-78192464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571725692	chr4:78192479-78192480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375860660	chr4:78192525-78192526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs148538478	chr4:78192559-78192560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574231429	chr4:78192570-78192571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576374536	chr4:78192575-78192576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542166272	chr4:78192586-78192587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182937884	chr4:78192646-78192647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74740369	chr4:78192655-78192656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372870386	chr4:78192679-78192680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549084096	chr4:78192687-78192688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545199704	chr4:78192701-78192702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142767846	chr4:78192719-78192720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150248017	chr4:78192778-78192779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72866471	chr4:78192786-78192787	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	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
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Oral squamous cell carcinoma	17134496	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78191000-78193600	Enhancers	Placenta	Placenta
2	chr4:78191000-78200000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:78193600-78205400	Weak transcription	Placenta	Placenta
4	chr4:78199600-78201200	Enhancers	HMEC	breast
5	chr4:78200000-78200800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:78200000-78201000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:78200000-78201000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:78200000-78201000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:78203200-78203600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:78203400-78203800	Enhancers	Adipose Nuclei	Adipose
11	chr4:78205200-78205600	Enhancers	HSMMtube	muscle
12	chr4:78205200-78205800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:78205400-78205800	Enhancers	Placenta	Placenta
14	chr4:78205800-78211600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:78210400-78210600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr4:78210600-78221800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:78213200-78214600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr4:78214400-78214600	Enhancers	Placenta	Placenta
19	chr4:78214600-78214800	Enhancers	H9 Cell Line	embryonic stem cell
20	chr4:78214600-78215200	Weak transcription	Placenta	Placenta
21	chr4:78215200-78216000	Enhancers	Placenta	Placenta
22	chr4:78219000-78222200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr4:78219600-78219800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:78219600-78219800	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
25	chr4:78219600-78219800	Enhancers	Primary hematopoietic stem cells	blood
26	chr4:78219600-78219800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr4:78219600-78219800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr4:78219800-78222400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr4:78221400-78221600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:78221400-78221800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr4:78221600-78222400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:78221600-78222800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:78221800-78222200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr4:78221800-78222400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr4:78221800-78222800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr4:78221800-78222800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr4:78221800-78222800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr4:78221800-78222800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr4:78221800-78222800	Enhancers	Stomach Mucosa	stomach
40	chr4:78222000-78222400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr4:78222000-78222400	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr4:78222000-78222600	Enhancers	Fetal Muscle Leg	muscle
43	chr4:78222000-78222600	Enhancers	HSMMtube	muscle
44	chr4:78222000-78223000	Enhancers	H1 Cell Line	embryonic stem cell
45	chr4:78222200-78222600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr4:78222200-78222600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr4:78222200-78222600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:78222200-78222600	Enhancers	Fetal Muscle Trunk	muscle
49	chr4:78222200-78222800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr4:78222200-78222800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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