Variant report

Variant	nsv595131
Chromosome Location	chr4:110165434-110220384
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	ATF1	chr4:110199643-110199855	K562	blood:	n/a	n/a
2	ATF1	chr4:110212188-110212416	K562	blood:	n/a	n/a
3	BACH1	chr4:110199801-110199974	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:110199756-110199987	K562	blood:	n/a	n/a
5	BATF	chr4:110197748-110197986	GM12878	blood:	n/a	n/a
6	BCL11A	chr4:110199725-110199944	GM12878	blood:	n/a	chr4:110199915-110199924 chr4:110199914-110199923
7	BCL11A	chr4:110199686-110199939	GM12878	blood:	n/a	chr4:110199915-110199924 chr4:110199914-110199923
8	BCL11A	chr4:110199992-110200202	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:110197689-110197963	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:110199665-110200327	GM12878	blood:	n/a	n/a
11	BRCA1	chr4:110178049-110178267	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr4:110212070-110212453	K562	blood:	n/a	n/a
13	CCNT2	chr4:110178115-110178269	K562	blood:	n/a	n/a
14	CEBPB	chr4:110217637-110218103	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:110209898-110209922	K562	blood:	n/a	n/a
16	CEBPB	chr4:110215720-110216115	Hela-S3	cervix:	n/a	n/a
17	CHD1	chr4:110215439-110215495	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr4:110197952-110198024	GM12878	blood:	n/a	n/a
19	CHD2	chr4:110215193-110215478	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr4:110199676-110200417	GM12878	blood:	n/a	n/a
21	CHD2	chr4:110197723-110198050	GM12878	blood:	n/a	n/a
22	CTCF	chr4:110219920-110220070	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr4:110215260-110215410	SAEC	small airway:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
24	CTCF	chr4:110215269-110215484	GM19238	blood:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
25	CTCF	chr4:110219940-110220090	Caco-2	colon:	n/a	n/a
26	CTCF	chr4:110219900-110220050	GM12869	blood:	n/a	n/a
27	CTCF	chr4:110219580-110219730	NHEK	skin:	n/a	n/a
28	CTCF	chr4:110219940-110220090	BJ	skin:	n/a	n/a
29	CTCF	chr4:110215300-110215450	MCF-7	breast:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
30	CTCF	chr4:110215340-110215490	GM12873	blood:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
31	CTCF	chr4:110215320-110215470	NHDF-neo	bronchial:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
32	CTCF	chr4:110215323-110215423	Pancreas_OC	pancreas:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
33	CTCF	chr4:110215360-110215510	HRE	kidney:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
34	CTCF	chr4:110215280-110215430	SK-N-SH_RA	brain:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
35	CTCF	chr4:110215239-110215511	K562	blood:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
36	CTCF	chr4:110215320-110215470	HL-60	blood:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
37	CTCF	chr4:110215400-110215550	HAc	cerebellar:	n/a	n/a
38	CTCF	chr4:110215240-110215390	AG04450	lung:	n/a	chr4:110215363-110215381
39	CTCF	chr4:110215280-110215430	AG10803	skin:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
40	CTCF	chr4:110215300-110215450	HCFaa	heart:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
41	CTCF	chr4:110219900-110220050	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr4:110215120-110215270	WI-38	lung:	n/a	n/a
43	CTCF	chr4:110215280-110215430	GM12867	blood:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
44	CTCF	chr4:110219820-110219970	HMEC	breast:	n/a	n/a
45	CTCF	chr4:110215300-110215450	Caco-2	colon:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
46	CTCF	chr4:110219880-110220030	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr4:110219900-110220050	NHEK	skin:	n/a	n/a
48	CTCF	chr4:110215320-110215470	HCPEpiC	choroid plexus:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381
49	CTCF	chr4:110219894-110220061	ProgFib	skin:	n/a	n/a
50	CTCF	chr4:110215280-110215430	GM12865	blood:	n/a	chr4:110215397-110215407 chr4:110215396-110215409 chr4:110215363-110215381

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:110220063-110220113	HUVEC	blood vessel:	n/a
2	chr4:110220063-110220113	Caco-2	colon:	n/a
3	chr4:110220063-110220113	HCPEpiC	choroid plexus:	n/a
4	chr4:110220063-110220113	MCF10A-Er-Src	breast:	n/a
5	chr4:110220063-110220113	T-47D	breast:	n/a
6	chr4:110220063-110220113	SK-N-MC	brain:	n/a
7	chr4:110220063-110220113	AG04449	skin:	fetal
8	chr4:110220063-110220113	SK-N-SH	brain:	n/a
9	chr4:110220063-110220113	PANC-1	pancreas:	n/a
10	chr4:110220063-110220113	HAEpiC	amniotic membrane:	n/a
11	chr4:110220063-110220113	AG10803	skin:	n/a
12	chr4:110220063-110220113	SAEC	small airway:	n/a
13	chr4:110220063-110220113	A549	lung:	n/a
14	chr4:110220063-110220113	U87	brain:	n/a
15	chr4:110220063-110220113	HIPEpiC	eye:	n/a
16	chr4:110220063-110220113	NHDF-neo	bronchial:	n/a
17	chr4:110220063-110220113	GM12892	blood:	n/a
18	chr4:110220063-110220113	Hela-S3	cervix:	n/a
19	chr4:110220063-110220113	Hepatocyte	liver:	n/a
20	chr4:110220063-110220113	HL-60	blood:	n/a
21	chr4:110220063-110220113	GM12878	blood:	n/a
22	chr4:110220063-110220113	HCT-116	colon:	n/a
23	chr4:110220063-110220113	H1-hESC	embryonic stem cell:	embryo
24	chr4:110220063-110220113	HCM	heart:	n/a
25	chr4:110220063-110220113	AG09309	skin:	n/a
26	chr4:110220063-110220113	GM12891	blood:	n/a
27	chr4:110220063-110220113	NB4	blood:	n/a
28	chr4:110220063-110220113	NH-A	brain:	n/a
29	chr4:110220063-110220113	HRCEpiC	kidney:	n/a
30	chr4:110220063-110220113	AG09319	gingival:	n/a
31	chr4:110220063-110220113	MCF-7	breast:	n/a
32	chr4:110220063-110220113	NHBE	bronchial:	n/a
33	chr4:110220063-110220113	AG04450	lung:	fetal
34	chr4:110220063-110220113	HRPEpiC	eye:	n/a
35	chr4:110220063-110220113	HNPCEpiC	eye:	n/a
36	chr4:110220063-110220113	ProgFib	skin:	n/a
37	chr4:110220063-110220113	CMK	blood:	n/a
38	chr4:110220063-110220113	HRE	kidney:	n/a
39	chr4:110220063-110220113	GM06990	blood:	n/a
40	chr4:110220063-110220113	BE2_C	brain:	n/a
41	chr4:110220063-110220113	GM19239	blood:	n/a
42	chr4:110220063-110220113	SKMC	muscle:	n/a
43	chr4:110220063-110220113	HCF	heart:	n/a
44	chr4:110220063-110220113	ECC-1	luminal epithelium:	n/a
45	chr4:110220063-110220113	IMR90	lung:	fetal
46	chr4:110220063-110220113	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:110220063-110220113	LNCaP	prostate:	n/a
48	chr4:110220063-110220113	HMEC	breast:	n/a
49	chr4:110220063-110220113	PrEC	prostate:	n/a
50	chr4:110220063-110220113	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:110081460..110082993-chr4:110163181..110166012,2	MCF-7	breast:
2	chr4:110200880..110202653-chr4:110203323..110206057,2	K562	blood:
3	chr4:110190667..110192285-chr4:110194984..110197043,2	K562	blood:
4	chr4:110200977..110202529-chr4:110206288..110208734,2	K562	blood:
5	chr4:110166617..110169295-chr4:110175450..110177402,2	K562	blood:
6	chr4:110171275..110172964-chr4:110180215..110181842,2	K562	blood:
7	chr4:110218896..110220451-chr4:110222507..110224229,2	K562	blood:
8	chr4:109997373..109998881-chr4:110214919..110216125,4	MCF-7	breast:
9	chr4:110202867..110205707-chr4:110206344..110210192,3	K562	blood:
10	chr4:110209292..110211256-chr4:110212349..110215176,2	K562	blood:
11	chr4:110203551..110205977-chr4:110206867..110209151,3	K562	blood:
12	chr4:109755575..109756625-chr4:110219552..110220537,7	MCF-7	breast:
13	chr4:110180243..110182937-chr4:110184044..110187466,3	K562	blood:
14	chr4:110218875..110221390-chr4:110226425..110229049,3	K562	blood:
15	chr4:110180243..110182937-chr4:110184044..110187466,3	K562	blood:
16	chr4:110190667..110192285-chr4:110194984..110197043,2	K562	blood:
17	chr4:110202867..110205707-chr4:110206344..110210192,3	K562	blood:
18	chr4:110205873..110208471-chr4:110210167..110212906,3	K562	blood:
19	chr4:110205873..110208471-chr4:110210167..110212906,3	K562	blood:
20	chr4:110203551..110205977-chr4:110206867..110209151,3	K562	blood:
21	chr4:109755705..109756568-chr4:110214904..110215406,2	K562	blood:
22	chr4:110209292..110211256-chr4:110212349..110215176,2	K562	blood:
23	chr4:109604835..109605458-chr4:110219549..110220243,2	MCF-7	breast:
24	chr4:109755660..109756630-chr4:110219482..110220438,3	MCF-7	breast:
25	chr4:110185597..110188349-chr4:110190065..110191993,2	K562	blood:
26	chr4:110206971..110209118-chr4:110210167..110212252,2	K562	blood:
27	chr4:110166617..110169295-chr4:110175450..110177402,2	K562	blood:
28	chr4:110206971..110209118-chr4:110210167..110212252,2	K562	blood:
29	chr4:110171275..110172964-chr4:110180215..110181842,2	K562	blood:
30	chr4:109996527..109997500-chr4:110219968..110220478,2	MCF-7	breast:
31	chr4:110200880..110202653-chr4:110203323..110206057,2	K562	blood:
32	chr4:109755609..109756369-chr4:110214925..110215856,2	MCF-7	breast:
33	chr4:110200977..110202529-chr4:110206288..110208734,2	K562	blood:
34	chr4:110185597..110188349-chr4:110190065..110191993,2	K562	blood:
35	chr4:109881894..109883700-chr4:110175971..110178071,2	K562	blood:
36	chr4:110160872..110163368-chr4:110165331..110168777,3	K562	blood:

Variant related genes	Relation type
ENSG00000246774	TF binding region
ENSG00000246774	CpG island
ENSG00000188517	chromatin interactions
ENSG00000246774	chromatin interactions

Extended variants
information (count: 1927 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1927 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10488877	chr4:110165434-110165435	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186483987	chr4:110165453-110165454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534273681	chr4:110165462-110165463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138072202	chr4:110165522-110165523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76325012	chr4:110165527-110165528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112574814	chr4:110165533-110165534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536734156	chr4:110165537-110165538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556369117	chr4:110165554-110165555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549878051	chr4:110165557-110165558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576227827	chr4:110165580-110165581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542157193	chr4:110165611-110165612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562006604	chr4:110165635-110165636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76452261	chr4:110165691-110165692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541040311	chr4:110165710-110165711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539661216	chr4:110165711-110165712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190124787	chr4:110165730-110165731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373507633	chr4:110165748-110165749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568291229	chr4:110165759-110165760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181736494	chr4:110165771-110165772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149138892	chr4:110165777-110165778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79901028	chr4:110165809-110165810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10030903	chr4:110165842-110165843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs529055991	chr4:110165886-110165887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549301411	chr4:110165926-110165927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144943978	chr4:110165930-110165931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187306100	chr4:110165978-110165979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376841310	chr4:110165981-110165982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551122728	chr4:110166010-110166011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78959089	chr4:110166033-110166034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536799084	chr4:110166052-110166053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75210198	chr4:110166182-110166183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576241854	chr4:110166213-110166214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10033402	chr4:110166241-110166242	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs190759023	chr4:110166265-110166266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555391038	chr4:110166332-110166333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556050483	chr4:110166367-110166368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77848554	chr4:110166418-110166419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573677800	chr4:110166465-110166466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2158469	chr4:110166505-110166506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs386678300	chr4:110166604-110166605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114578516	chr4:110166605-110166606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs386678301	chr4:110166615-110166616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184896382	chr4:110166616-110166617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563725522	chr4:110166724-110166725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6836171	chr4:110166732-110166733	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs549164409	chr4:110166755-110166756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539053990	chr4:110166773-110166774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559481843	chr4:110166793-110166794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528404695	chr4:110166851-110166852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189710245	chr4:110166867-110166868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	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
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Schizophrenia	19546859	CNVD
Colorectal cancer	16272173	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110155200-110192200	Weak transcription	Hela-S3	cervix
2	chr4:110164800-110165600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:110165200-110171400	Weak transcription	HSMM	muscle
4	chr4:110165400-110171200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:110169400-110170200	Enhancers	HSMMtube	muscle
6	chr4:110171000-110186800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr4:110171200-110173400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr4:110171400-110172600	Strong transcription	HSMM	muscle
9	chr4:110172000-110173600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr4:110172400-110173200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:110172600-110172800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr4:110172600-110185000	Weak transcription	HSMM	muscle
13	chr4:110184800-110185000	Enhancers	Psoas Muscle	Psoas
14	chr4:110184800-110185200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:110184800-110185600	Enhancers	K562	blood
16	chr4:110184800-110185800	Enhancers	Brain Anterior Caudate	brain
17	chr4:110185000-110185400	Enhancers	HSMM	muscle
18	chr4:110185000-110185800	Enhancers	HSMMtube	muscle
19	chr4:110185200-110185600	Enhancers	Muscle Satellite Cultured Cells	--
20	chr4:110185200-110185600	Enhancers	Brain Hippocampus Middle	brain
21	chr4:110185200-110186200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:110185400-110185600	Enhancers	Aorta	Aorta
23	chr4:110185400-110185800	Flanking Active TSS	HSMM	muscle
24	chr4:110185600-110185800	Enhancers	Psoas Muscle	Psoas
25	chr4:110185600-110186800	Weak transcription	K562	blood
26	chr4:110185800-110186000	Enhancers	HSMM	muscle
27	chr4:110185800-110186400	Weak transcription	HSMMtube	muscle
28	chr4:110186000-110215200	Weak transcription	HSMM	muscle
29	chr4:110186200-110188400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr4:110186400-110186600	Enhancers	HSMMtube	muscle
31	chr4:110186600-110186800	Bivalent Enhancer	Fetal Brain Male	brain
32	chr4:110186800-110187000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr4:110186800-110187200	Enhancers	K562	blood
34	chr4:110188400-110189400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr4:110189400-110189600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:110189600-110196200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:110192200-110194000	Strong transcription	Hela-S3	cervix
38	chr4:110194000-110196600	Weak transcription	Hela-S3	cervix
39	chr4:110196000-110196400	Enhancers	Brain Substantia Nigra	brain
40	chr4:110196000-110196600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:110196000-110196600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr4:110196000-110197000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr4:110196000-110197200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:110196200-110196400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr4:110196200-110196800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:110196200-110197000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr4:110196200-110197000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr4:110196200-110197000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr4:110196200-110197200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:110196200-110197400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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