Variant report

Variant	nsv917053
Chromosome Location	chr4:147265436-147499653
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1777)
CpG islands
(count:1831)
Chromatin interactive
region (count:66)
LncRNA
region (count:4)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1777 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:147442767-147443252	K562	blood:	n/a	n/a
2	ARID3A	chr4:147441861-147442445	K562	blood:	n/a	n/a
3	ARID3A	chr4:147300799-147301269	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:147328607-147329350	K562	blood:	n/a	n/a
5	ARID3A	chr4:147443477-147443775	HepG2	liver:	n/a	chr4:147443637-147443645
6	ARID3A	chr4:147442013-147442422	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:147442908-147443108	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:147444301-147444570	K562	blood:	n/a	n/a
9	ATF1	chr4:147446984-147447324	K562	blood:	n/a	n/a
10	ATF1	chr4:147443041-147443754	K562	blood:	n/a	n/a
11	ATF1	chr4:147328796-147329286	K562	blood:	n/a	n/a
12	ATF1	chr4:147432386-147432914	K562	blood:	n/a	n/a
13	ATF2	chr4:147443414-147443788	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr4:147371514-147372128	GM12878	blood:	n/a	n/a
15	ATF2	chr4:147379696-147380346	GM12878	blood:	n/a	n/a
16	ATF2	chr4:147443319-147443835	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr4:147442030-147442543	GM12878	blood:	n/a	n/a
18	ATF2	chr4:147379548-147380300	GM12878	blood:	n/a	n/a
19	ATF2	chr4:147442673-147443886	GM12878	blood:	n/a	n/a
20	ATF2	chr4:147442765-147443790	GM12878	blood:	n/a	n/a
21	ATF3	chr4:147466307-147466599	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr4:147466340-147466550	K562	blood:	n/a	n/a
23	BACH1	chr4:147443489-147443835	K562	blood:	n/a	n/a
24	BACH1	chr4:147482036-147482054	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr4:147353224-147353490	K562	blood:	n/a	n/a
26	BACH1	chr4:147442165-147442357	K562	blood:	n/a	n/a
27	BACH1	chr4:147443429-147444146	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr4:147442922-147443161	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr4:147427472-147427738	GM12878	blood:	n/a	chr4:147427561-147427572
30	BATF	chr4:147407141-147407403	GM12878	blood:	n/a	n/a
31	BATF	chr4:147379769-147380125	GM12878	blood:	n/a	n/a
32	BATF	chr4:147371529-147372021	GM12878	blood:	n/a	chr4:147371988-147371996
33	BATF	chr4:147407128-147407443	GM12878	blood:	n/a	n/a
34	BATF	chr4:147443412-147443659	GM12878	blood:	n/a	n/a
35	BCLAF1	chr4:147379664-147380144	GM12878	blood:	n/a	n/a
36	BCLAF1	chr4:147442723-147443838	GM12878	blood:	n/a	n/a
37	BHLHE40	chr4:147407200-147407400	GM12878	blood:	n/a	n/a
38	BHLHE40	chr4:147444128-147444393	K562	blood:	n/a	n/a
39	BHLHE40	chr4:147442029-147443756	GM12878	blood:	n/a	chr4:147443156-147443172
40	BHLHE40	chr4:147442084-147443706	K562	blood:	n/a	chr4:147443156-147443172
41	BHLHE40	chr4:147432566-147432820	K562	blood:	n/a	n/a
42	BHLHE40	chr4:147432755-147432758	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:147328854-147329449	K562	blood:	n/a	n/a
44	BHLHE40	chr4:147447001-147447424	K562	blood:	n/a	n/a
45	BRCA1	chr4:147443384-147443730	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr4:147442894-147443193	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr4:147443404-147443704	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr4:147443151-147443699	HepG2	liver:	n/a	n/a
49	BRCA1	chr4:147443445-147443723	GM12878	blood:	n/a	n/a
50	CBX3	chr4:147328767-147329372	K562	blood:	n/a	n/a

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:147442789-147442839	Jurkat	blood:	n/a
2	chr4:147442789-147442839	Jurkat	blood:	n/a
3	chr4:147443209-147443259	IMR90	lung:	fetal
4	chr4:147443002-147443052	HIPEpiC	eye:	n/a
5	chr4:147443742-147443792	BE2_C	brain:	n/a
6	chr4:147443742-147443792	Hepatocyte	liver:	n/a
7	chr4:147443996-147444046	NHBE	bronchial:	n/a
8	chr4:147417332-147417382	AG09309	skin:	n/a
9	chr4:147366475-147366525	AG04450	lung:	fetal
10	chr4:147417332-147417382	A549	lung:	n/a
11	chr4:147366958-147367008	NHDF-neo	bronchial:	n/a
12	chr4:147366592-147366642	HCT-116	colon:	n/a
13	chr4:147443257-147443307	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:147442789-147442839	RPTEC	kidney:	n/a
15	chr4:147367017-147367067	NH-A	brain:	n/a
16	chr4:147443237-147443287	NHBE	bronchial:	n/a
17	chr4:147366744-147366794	GM12892	blood:	n/a
18	chr4:147364608-147364658	AG10803	skin:	n/a
19	chr4:147443703-147443753	K562	blood:	n/a
20	chr4:147366958-147367008	Hela-S3	cervix:	n/a
21	chr4:147366475-147366525	H1-hESC	embryonic stem cell:	embryo
22	chr4:147443662-147443712	HMEC	breast:	n/a
23	chr4:147366958-147367008	SKMC	muscle:	n/a
24	chr4:147366744-147366794	Hela-S3	cervix:	n/a
25	chr4:147442738-147442788	H1-hESC	embryonic stem cell:	embryo
26	chr4:147443215-147443265	MCF-7	breast:	n/a
27	chr4:147442738-147442788	AG04450	lung:	fetal
28	chr4:147366592-147366642	GM12892	blood:	n/a
29	chr4:147443478-147443528	HMEC	breast:	n/a
30	chr4:147393712-147393762	HRE	kidney:	n/a
31	chr4:147287029-147287079	AG09319	gingival:	n/a
32	chr4:147287029-147287079	HAEpiC	amniotic membrane:	n/a
33	chr4:147287029-147287079	Jurkat	blood:	n/a
34	chr4:147366744-147366794	T-47D	breast:	n/a
35	chr4:147443489-147443539	ovcar-3	ovarian:	n/a
36	chr4:147443489-147443539	A549	lung:	n/a
37	chr4:147443215-147443265	HMEC	breast:	n/a
38	chr4:147393712-147393762	GM19239	blood:	n/a
39	chr4:147366592-147366642	T-47D	breast:	n/a
40	chr4:147417332-147417382	GM12892	blood:	n/a
41	chr4:147443489-147443539	ProgFib	skin:	n/a
42	chr4:147443721-147443771	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:147442738-147442788	GM12878	blood:	n/a
44	chr4:147417332-147417382	ProgFib	skin:	n/a
45	chr4:147417332-147417382	ECC-1	luminal epithelium:	n/a
46	chr4:147443489-147443539	HRCEpiC	kidney:	n/a
47	chr4:147366475-147366525	GM12891	blood:	n/a
48	chr4:147366475-147366525	Hela-S3	cervix:	n/a
49	chr4:147443209-147443259	MCF-7	breast:	n/a
50	chr4:147443721-147443771	HAEpiC	amniotic membrane:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:147417283..147419141-chr4:147422928..147424810,2	K562	blood:
2	chr4:147488323..147490035-chr4:147830960..147833079,2	MCF-7	breast:
3	chr4:147419888..147422305-chr4:147440124..147442502,3	K562	blood:
4	chr4:147277196..147280652-chr4:147297351..147300192,3	K562	blood:
5	chr4:147304920..147306569-chr4:147316021..147318910,2	K562	blood:
6	chr4:147444230..147446047-chr4:147464429..147467416,2	K562	blood:
7	chr4:147440616..147443246-chr4:147445900..147447774,2	MCF-7	breast:
8	chr4:147428018..147430283-chr4:147430558..147433344,2	MCF-7	breast:
9	chr4:147304920..147306569-chr4:147316021..147318910,2	K562	blood:
10	chr4:147429465..147431339-chr4:147443372..147446035,2	MCF-7	breast:
11	chr4:147429465..147431339-chr4:147443372..147446035,2	MCF-7	breast:
12	chr4:147298326..147300509-chr4:147303164..147305825,2	K562	blood:
13	chr4:147377292..147378986-chr4:147382091..147384847,2	K562	blood:
14	chr4:147313367..147315666-chr4:147317925..147320172,2	K562	blood:
15	chr4:147284742..147287681-chr4:147296749..147298295,2	K562	blood:
16	chr4:147429340..147431925-chr4:147435068..147436668,2	K562	blood:
17	chr4:147433100..147434679-chr4:147439045..147441227,2	K562	blood:
18	chr4:147277196..147280652-chr4:147297351..147300192,3	K562	blood:
19	chr4:147422785..147424738-chr4:147428828..147431211,2	K562	blood:
20	chr4:147428018..147430283-chr4:147430558..147433344,2	MCF-7	breast:
21	chr4:147396542..147399572-chr4:147441931..147444367,3	K562	blood:
22	chr4:147418770..147421708-chr4:147429098..147431624,2	K562	blood:
23	chr4:147414219..147415892-chr4:147439502..147441061,2	K562	blood:
24	chr4:147418770..147421708-chr4:147429098..147431624,2	K562	blood:
25	chr4:147431194..147433726-chr4:147442106..147444306,2	MCF-7	breast:
26	chr4:147392612..147394631-chr4:147558552..147560059,2	K562	blood:
27	chr4:147417660..147419201-chr4:147441419..147443363,2	K562	blood:
28	chr4:147429340..147432833-chr4:147435168..147439356,4	K562	blood:
29	chr4:147329344..147331029-chr4:147426508..147428217,2	K562	blood:
30	chr4:147434896..147436874-chr4:147440310..147443496,4	K562	blood:
31	chr4:147331330..147334198-chr4:147335520..147338356,2	K562	blood:
32	chr4:147437110..147440734-chr4:147441059..147444351,6	K562	blood:
33	chr4:147329344..147331029-chr4:147426508..147428217,2	K562	blood:
34	chr4:147430052..147432471-chr4:147442517..147444905,3	K562	blood:
35	chr4:147284742..147287681-chr4:147296749..147298295,2	K562	blood:
36	chr4:147377292..147378986-chr4:147382091..147384847,2	K562	blood:
37	chr4:147433100..147434679-chr4:147439045..147441227,2	K562	blood:
38	chr4:147414219..147415892-chr4:147439502..147441061,2	K562	blood:
39	chr4:147438639..147441130-chr4:147443226..147445590,2	MCF-7	breast:
40	chr4:147422785..147424738-chr4:147428828..147431211,2	K562	blood:
41	chr4:147444230..147446047-chr4:147464429..147467416,2	K562	blood:
42	chr4:147419888..147422305-chr4:147440124..147442502,3	K562	blood:
43	chr4:147280177..147282704-chr4:147285099..147286866,2	MCF-7	breast:
44	chr4:147362840..147364898-chr4:147369534..147371041,2	K562	blood:
45	chr4:147417283..147419141-chr4:147422928..147424810,2	K562	blood:
46	chr4:147430052..147432364-chr4:147442835..147444905,2	K562	blood:
47	chr4:147331330..147334198-chr4:147335520..147338356,2	K562	blood:
48	chr4:147364033..147364846-chr9:111458384..111458949,2	MCF-7	breast:
49	chr4:147316149..147318201-chr4:147333112..147335768,2	K562	blood:
50	chr4:147362840..147364898-chr4:147369534..147371041,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-6L6.2.1-4	chr4:147340612-147340680	l_2750_chr4:147340611-147343049_adipose
2	lnc-RP11-6L6.2.1-4	chr4:147342836-147343049	l_2750_chr4:147340611-147343049_adipose
3	lnc-TTC29-1	chr4:147425001-147425055	NONHSAT098669
4	lnc-TTC29-1	chr4:147399031-147399453	NONHSAT098669

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7849-3p	chr4:147329798-147329819	MIMAT0030424

No data

Variant related genes	Relation type
RNU1-44P	TF binding region
SLC10A7	TF binding region
RNU1-44P	CpG island
SLC10A7	CpG island
ENSG00000151615	chromatin interactions
ENSG00000120519	chromatin interactions

Extended variants
information (count: 6655 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:6655 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555812370	chr4:147265487-147265488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs75447511	chr4:147265493-147265494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148155533	chr4:147265505-147265506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559241033	chr4:147265528-147265529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183481153	chr4:147265537-147265538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527660450	chr4:147265561-147265562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558956730	chr4:147265565-147265566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188158150	chr4:147265566-147265567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563383161	chr4:147265594-147265595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530722562	chr4:147265634-147265635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs17021396	chr4:147265650-147265651	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs561812228	chr4:147265653-147265654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531020644	chr4:147265663-147265664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552326452	chr4:147265692-147265693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142009273	chr4:147265707-147265708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533633883	chr4:147265711-147265712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547299555	chr4:147265723-147265724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181173688	chr4:147265737-147265738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544137963	chr4:147265772-147265773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146112790	chr4:147265841-147265842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564934399	chr4:147265846-147265847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528099846	chr4:147265866-147265867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138970519	chr4:147265869-147265870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570917572	chr4:147265922-147265923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28625764	chr4:147265930-147265931	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs142024846	chr4:147265951-147265952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539374965	chr4:147265978-147265979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs61219941	chr4:147266004-147266005	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs79136710	chr4:147266035-147266036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372814403	chr4:147266125-147266126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541769687	chr4:147266127-147266128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555174298	chr4:147266208-147266209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575272850	chr4:147266245-147266246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74864749	chr4:147266267-147266268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564705643	chr4:147266272-147266273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184941262	chr4:147266325-147266326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540975941	chr4:147266382-147266383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560760236	chr4:147266398-147266399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375998591	chr4:147266399-147266400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529271514	chr4:147266410-147266411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549327713	chr4:147266432-147266433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376209549	chr4:147266461-147266462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569265331	chr4:147266469-147266470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146340844	chr4:147266547-147266548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551561006	chr4:147266550-147266551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570359284	chr4:147266555-147266556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369494340	chr4:147266598-147266599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539238986	chr4:147266637-147266638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552858806	chr4:147266723-147266724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566382331	chr4:147266727-147266728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21633010	CNVD
Breast cancer	20393555	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1826 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147241800-147284800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr4:147264600-147265800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr4:147264800-147267000	Weak transcription	GM12878-XiMat	blood
4	chr4:147265400-147270400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:147267000-147267200	Enhancers	GM12878-XiMat	blood
6	chr4:147267200-147267600	Flanking Active TSS	GM12878-XiMat	blood
7	chr4:147267600-147268600	Enhancers	GM12878-XiMat	blood
8	chr4:147268200-147268800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:147268200-147269600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:147268200-147269800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:147268400-147270600	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr4:147270200-147270800	Enhancers	NHEK	skin
13	chr4:147270200-147271000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:147270400-147270800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr4:147270600-147271600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:147270800-147271000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:147270800-147271200	Active TSS	NHEK	skin
18	chr4:147270800-147271600	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr4:147270800-147271600	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr4:147270800-147271600	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr4:147270800-147271600	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr4:147270800-147271600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:147271000-147271200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:147271000-147271400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr4:147271000-147271400	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr4:147271000-147271600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr4:147271000-147271600	Active TSS	H1 Cell Line	embryonic stem cell
28	chr4:147271000-147271600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr4:147271000-147271600	Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr4:147271000-147271600	Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr4:147271000-147271600	Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr4:147271000-147271600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:147271200-147271600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:147271200-147271600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:147271200-147271600	Active TSS	H9 Cell Line	embryonic stem cell
36	chr4:147271200-147271600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr4:147271200-147271600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:147271200-147271600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr4:147271600-147281600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:147276200-147292400	Weak transcription	Aorta	Aorta
41	chr4:147277200-147281000	Weak transcription	Primary B cells from cord blood	blood
42	chr4:147277400-147314200	Weak transcription	Left Ventricle	heart
43	chr4:147277600-147287000	Weak transcription	Small Intestine	intestine
44	chr4:147281000-147282800	Strong transcription	Primary B cells from cord blood	blood
45	chr4:147281600-147282600	Weak transcription	Fetal Intestine Large	intestine
46	chr4:147281600-147282800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr4:147281600-147284000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr4:147282600-147282800	ZNF genes & repeats	Fetal Intestine Large	intestine
49	chr4:147282600-147282800	ZNF genes & repeats	Pancreas	Pancrea
50	chr4:147282800-147283000	ZNF genes & repeats	Primary B cells from cord blood	blood

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