Variant report

Variant	nsv4404
Chromosome Location	chr4:82340986-82386148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:323)
CpG islands
(count:550)
Chromatin interactive
region (count:28)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:82342499-82343466	K562	blood:	n/a	n/a
2	ARID3A	chr4:82375769-82376300	K562	blood:	n/a	n/a
3	ATF1	chr4:82342595-82343231	K562	blood:	n/a	n/a
4	ATF1	chr4:82363683-82363911	K562	blood:	n/a	n/a
5	ATF1	chr4:82375619-82376047	K562	blood:	n/a	n/a
6	ATF2	chr4:82342484-82343053	GM12878	blood:	n/a	n/a
7	ATF3	chr4:82375629-82376009	K562	blood:	n/a	n/a
8	ATF3	chr4:82342472-82343073	K562	blood:	n/a	n/a
9	ATF3	chr4:82375746-82375953	K562	blood:	n/a	n/a
10	BACH1	chr4:82342648-82343445	K562	blood:	n/a	n/a
11	BACH1	chr4:82369142-82369334	K562	blood:	n/a	n/a
12	BACH1	chr4:82375779-82375893	K562	blood:	n/a	n/a
13	BATF	chr4:82342612-82342992	GM12878	blood:	n/a	chr4:82342803-82342812 chr4:82342791-82342801 chr4:82342787-82342797 chr4:82342790-82342801
14	BATF	chr4:82342610-82342946	GM12878	blood:	n/a	chr4:82342803-82342812 chr4:82342791-82342801 chr4:82342787-82342797 chr4:82342790-82342801
15	BATF	chr4:82343802-82344096	GM12878	blood:	n/a	n/a
16	BATF	chr4:82343728-82344077	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:82342679-82342966	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:82343813-82343967	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:82369110-82369397	K562	blood:	n/a	n/a
20	BHLHE40	chr4:82342487-82343338	K562	blood:	n/a	n/a
21	BHLHE40	chr4:82374733-82375091	K562	blood:	n/a	n/a
22	CBX3	chr4:82342417-82343460	K562	blood:	n/a	n/a
23	CBX3	chr4:82375509-82376026	K562	blood:	n/a	n/a
24	CBX3	chr4:82342440-82343147	K562	blood:	n/a	n/a
25	CCNT2	chr4:82342603-82343344	K562	blood:	n/a	chr4:82343058-82343067
26	CEBPB	chr4:82342585-82343140	K562	blood:	n/a	n/a
27	CEBPB	chr4:82351776-82351950	HepG2	liver:	n/a	chr4:82351825-82351836
28	CEBPB	chr4:82342538-82343133	K562	blood:	n/a	n/a
29	CEBPB	chr4:82342693-82342941	K562	blood:	n/a	n/a
30	CEBPD	chr4:82342537-82343287	K562	blood:	n/a	n/a
31	CEBPD	chr4:82342472-82343388	K562	blood:	n/a	n/a
32	CHD2	chr4:82342515-82343188	K562	blood:	n/a	n/a
33	CREB1	chr4:82375534-82376143	K562	blood:	n/a	n/a
34	CREB1	chr4:82342370-82343194	K562	blood:	n/a	n/a
35	CTCF	chr4:82346245-82346660	K562	blood:	n/a	n/a
36	CTCF	chr4:82346300-82346450	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr4:82346380-82346530	K562	blood:	n/a	n/a
38	CTCF	chr4:82346354-82346545	K562	blood:	n/a	n/a
39	CTCF	chr4:82354489-82354758	K562	blood:	n/a	n/a
40	CTCF	chr4:82374680-82374830	NHEK	skin:	n/a	n/a
41	CTCF	chr4:82368692-82368757	Lung_OC	lung:	n/a	n/a
42	CTCF	chr4:82343642-82343732	K562	blood:	n/a	n/a
43	CTCF	chr4:82346308-82346570	K562	blood:	n/a	n/a
44	CTCF	chr4:82378293-82378312	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr4:82364580-82364730	HRE	kidney:	n/a	n/a
46	CTCF	chr4:82382700-82382850	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr4:82382050-82382139	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr4:82354589-82354637	K562	blood:	n/a	n/a
49	CUX1	chr4:82375688-82375919	K562	blood:	n/a	n/a
50	CUX1	chr4:82353511-82353514	K562	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:82373104-82373154	HUVEC	blood vessel:	n/a
2	chr4:82373104-82373154	HUVEC	blood vessel:	n/a
3	chr4:82375718-82375768	MCF-7	breast:	n/a
4	chr4:82367672-82367722	NHBE	bronchial:	n/a
5	chr4:82367672-82367722	SK-N-SH_RA	brain:	n/a
6	chr4:82362415-82362465	HEEpiC	esophagus:	n/a
7	chr4:82373104-82373154	HRPEpiC	eye:	n/a
8	chr4:82373104-82373154	CMK	blood:	n/a
9	chr4:82375718-82375768	HPAEpiC	pulmonary alveolar:	n/a
10	chr4:82373104-82373154	Caco-2	colon:	n/a
11	chr4:82373104-82373154	AG09319	gingival:	n/a
12	chr4:82348507-82348557	AG09309	skin:	n/a
13	chr4:82373104-82373154	AG09309	skin:	n/a
14	chr4:82367672-82367722	SKMC	muscle:	n/a
15	chr4:82350842-82350892	IMR90	lung:	fetal
16	chr4:82373104-82373154	Hela-S3	cervix:	n/a
17	chr4:82350883-82350933	Hepatocyte	liver:	n/a
18	chr4:82362415-82362465	HCF	heart:	n/a
19	chr4:82373104-82373154	IMR90	lung:	fetal
20	chr4:82367672-82367722	AG04449	skin:	fetal
21	chr4:82350842-82350892	HepG2	liver:	n/a
22	chr4:82373104-82373154	Jurkat	blood:	n/a
23	chr4:82348507-82348557	HMEC	breast:	n/a
24	chr4:82373104-82373154	SKMC	muscle:	n/a
25	chr4:82350842-82350892	GM06990	blood:	n/a
26	chr4:82375718-82375768	HL-60	blood:	n/a
27	chr4:82367672-82367722	HEK293	kidney:	embryo
28	chr4:82373104-82373154	AG10803	skin:	n/a
29	chr4:82362415-82362465	HRE	kidney:	n/a
30	chr4:82362415-82362465	NHBE	bronchial:	n/a
31	chr4:82367672-82367722	HIPEpiC	eye:	n/a
32	chr4:82348507-82348557	AG10803	skin:	n/a
33	chr4:82351016-82351066	GM06990	blood:	n/a
34	chr4:82351016-82351066	SAEC	small airway:	n/a
35	chr4:82373104-82373154	PFSK-1	brain:	n/a
36	chr4:82350842-82350892	Jurkat	blood:	n/a
37	chr4:82375718-82375768	HRPEpiC	eye:	n/a
38	chr4:82362415-82362465	HNPCEpiC	eye:	n/a
39	chr4:82346163-82346213	SK-N-SH_RA	brain:	n/a
40	chr4:82350883-82350933	IMR90	lung:	fetal
41	chr4:82351016-82351066	HUVEC	blood vessel:	n/a
42	chr4:82350842-82350892	ProgFib	skin:	n/a
43	chr4:82362415-82362465	AG10803	skin:	n/a
44	chr4:82348507-82348557	HIPEpiC	eye:	n/a
45	chr4:82373104-82373154	GM06990	blood:	n/a
46	chr4:82351016-82351066	HRCEpiC	kidney:	n/a
47	chr4:82375718-82375768	GM12891	blood:	n/a
48	chr4:82346163-82346213	HepG2	liver:	n/a
49	chr4:82350883-82350933	PFSK-1	brain:	n/a
50	chr4:82367672-82367722	HCF	heart:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:82342653..82344315-chr4:82756584..82758105,2	K562	blood:
2	chr4:82338718..82341149-chr4:82343228..82345190,2	K562	blood:
3	chr4:82341314..82344179-chr4:82360678..82363894,3	K562	blood:
4	chr4:82341740..82344236-chr4:82345813..82347931,2	MCF-7	breast:
5	chr4:82345669..82347516-chr4:82348800..82350865,2	K562	blood:
6	chr4:82327129..82328804-chr4:82341208..82343737,2	K562	blood:
7	chr4:82381521..82383255-chr4:82777347..82779912,2	MCF-7	breast:
8	chr4:82343748..82345292-chr4:82377281..82379980,2	K562	blood:
9	chr4:82342860..82344646-chr4:82347755..82350982,3	K562	blood:
10	chr4:82381811..82384214-chr4:82385052..82387248,2	K562	blood:
11	chr4:82340135..82342826-chr4:82350602..82352367,3	K562	blood:
12	chr4:82342729..82344646-chr4:82349482..82351498,2	K562	blood:
13	chr4:82381811..82384214-chr4:82385052..82387248,2	K562	blood:
14	chr4:82361014..82362993-chr4:82366245..82367851,2	K562	blood:
15	chr4:82327000..82327810-chr4:82341931..82342605,2	K562	blood:
16	chr4:82337897..82339898-chr4:82380969..82382702,2	K562	blood:
17	chr4:82342860..82344646-chr4:82347755..82350982,3	K562	blood:
18	chr4:82342729..82344646-chr4:82349482..82351498,2	K562	blood:
19	chr4:82341314..82344179-chr4:82360678..82363894,3	K562	blood:
20	chr4:82361014..82362993-chr4:82366245..82367851,2	K562	blood:
21	chr4:82330902..82334984-chr4:82339313..82344776,5	K562	blood:
22	chr4:82338718..82341149-chr4:82343228..82345190,2	K562	blood:
23	chr4:82340135..82342826-chr4:82350602..82352367,3	K562	blood:
24	chr4:82326927..82327852-chr4:82345884..82346881,4	K562	blood:
25	chr4:82341740..82344236-chr4:82345813..82347931,2	MCF-7	breast:
26	chr4:82332819..82334854-chr4:82340131..82342446,3	K562	blood:
27	chr4:82385615..82387164-chr4:82392080..82394570,2	K562	blood:
28	chr4:82345669..82347516-chr4:82348800..82350865,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGEF1B-1	chr4:82380633-82380668	ENSG00000251331.1

No data

Variant related genes	Relation type
RASGEF1B	TF binding region
RASGEF1B	CpG island
ENSG00000138670	chromatin interactions

Extended variants
information (count: 1605 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1605 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570902617	chr4:82340989-82340990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs112345947	chr4:82340995-82340996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550605443	chr4:82341033-82341034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527931454	chr4:82341037-82341038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6849758	chr4:82341061-82341062	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs536013909	chr4:82341162-82341163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114679174	chr4:82341167-82341168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529381775	chr4:82341175-82341176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11937878	chr4:82341261-82341262	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs148156251	chr4:82341265-82341266	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs141953398	chr4:82341273-82341274	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs75398327	chr4:82341342-82341343	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs150661429	chr4:82341343-82341344	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs558070663	chr4:82341369-82341370	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs543454046	chr4:82341371-82341372	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs76149529	chr4:82341416-82341417	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs11934269	chr4:82341499-82341500	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs17005134	chr4:82341520-82341521	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs566260163	chr4:82341521-82341522	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs559121965	chr4:82341526-82341527	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs533616625	chr4:82341560-82341561	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs182385350	chr4:82341585-82341586	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs544863958	chr4:82341596-82341597	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs564839588	chr4:82341600-82341601	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs386676579	chr4:82341608-82341609	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs557288394	chr4:82341668-82341669	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs17005135	chr4:82341675-82341676	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs186112881	chr4:82341678-82341679	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs550322243	chr4:82341710-82341711	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs116607730	chr4:82341805-82341806	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs75616749	chr4:82341839-82341840	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs369188025	chr4:82341881-82341882	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs111347914	chr4:82341911-82341912	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs546762472	chr4:82341920-82341921	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs146760127	chr4:82341953-82341954	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs148896348	chr4:82341981-82341982	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs558445282	chr4:82341989-82341990	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs552594727	chr4:82342001-82342002	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs572919625	chr4:82342007-82342008	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs571866511	chr4:82342012-82342013	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs557676594	chr4:82342022-82342023	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs113568250	chr4:82342063-82342064	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs372166407	chr4:82342089-82342090	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs191068117	chr4:82342109-82342110	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs557059335	chr4:82342112-82342113	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs34797554	chr4:82342170-82342171	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs574027953	chr4:82342192-82342193	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs142632878	chr4:82342196-82342197	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs150980285	chr4:82342213-82342214	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs10013789	chr4:82342225-82342226	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Myelodysplastic syndrome	18508791	CNVD
abnormal development	18461090	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1187 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:82332800-82341200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:82333200-82342600	Weak transcription	Brain Angular Gyrus	brain
3	chr4:82334400-82342800	Weak transcription	Brain Substantia Nigra	brain
4	chr4:82335000-82345600	Weak transcription	Aorta	Aorta
5	chr4:82338400-82341200	Enhancers	K562	blood
6	chr4:82339400-82350000	Weak transcription	Gastric	stomach
7	chr4:82339600-82342600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:82339600-82343000	Weak transcription	Small Intestine	intestine
9	chr4:82339800-82342400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr4:82340000-82342000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr4:82340200-82342200	Weak transcription	Stomach Mucosa	stomach
12	chr4:82340200-82342600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr4:82340200-82342600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr4:82340200-82345600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:82340400-82341200	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr4:82340400-82342400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr4:82340400-82342400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr4:82340400-82342600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr4:82340600-82341000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr4:82340600-82346600	Weak transcription	Primary T cells from cord blood	blood
21	chr4:82340800-82341000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:82341000-82341200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:82341000-82350600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:82341200-82341400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:82341200-82342600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr4:82341200-82343400	Flanking Active TSS	K562	blood
27	chr4:82341200-82344000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr4:82341200-82344000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr4:82341200-82344200	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr4:82341400-82342600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:82341600-82344200	Enhancers	Primary B cells from peripheral blood	blood
32	chr4:82342000-82342400	Enhancers	Primary B cells from cord blood	blood
33	chr4:82342000-82344200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr4:82342000-82344400	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr4:82342000-82347400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:82342200-82344000	Enhancers	Stomach Mucosa	stomach
37	chr4:82342400-82342600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr4:82342400-82342800	Weak transcription	Primary B cells from cord blood	blood
39	chr4:82342400-82343000	Enhancers	Duodenum Mucosa	Duodenum
40	chr4:82342400-82343400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr4:82342400-82343400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:82342400-82343400	Enhancers	Fetal Intestine Large	intestine
43	chr4:82342400-82343600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr4:82342400-82344000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr4:82342400-82344000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr4:82342400-82344000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr4:82342400-82344000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr4:82342400-82344000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr4:82342400-82344000	Enhancers	Fetal Intestine Small	intestine
50	chr4:82342400-82348600	Enhancers	NHEK	skin

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