Variant report

Variant	nsv537288
Chromosome Location	chr4:143884298-144010784
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:728)
CpG islands
(count:61)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:728 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:143906529-143906643	HepG2	liver:	n/a	n/a
2	BACH1	chr4:143946228-143946800	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:143946252-143946526	GM12878	blood:	n/a	chr4:143946422-143946433
4	BATF	chr4:143942530-143942886	GM12878	blood:	n/a	n/a
5	BATF	chr4:143942531-143942863	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:143994101-143994135	K562	blood:	n/a	n/a
7	BRCA1	chr4:143906226-143906612	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr4:143990215-143990486	K562	blood:	n/a	chr4:143990383-143990394
9	CEBPB	chr4:143957621-143957929	MCF-7	breast:	n/a	n/a
10	CEBPB	chr4:144003938-144004253	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:144010523-144010781	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr4:144003941-144004242	A549	lung:	n/a	n/a
13	CEBPB	chr4:144004785-144005093	Hela-S3	cervix:	n/a	chr4:144004855-144004872
14	CEBPB	chr4:143947235-143947385	A549	lung:	n/a	chr4:143947312-143947323
15	CEBPB	chr4:143944802-143945077	A549	lung:	n/a	n/a
16	CEBPB	chr4:143990289-143990526	IMR90	lung:	n/a	chr4:143990383-143990394
17	CEBPB	chr4:143947157-143947447	HepG2	liver:	n/a	chr4:143947312-143947323
18	CEBPB	chr4:143944806-143945035	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr4:143984737-143984932	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:143905861-143906636	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr4:143984634-143984998	HCT-116	colon:	n/a	n/a
22	CEBPB	chr4:143885951-143886043	IMR90	lung:	n/a	chr4:143886009-143886020 chr4:143886009-143886018 chr4:143886007-143886020
23	CEBPB	chr4:143990213-143990556	HepG2	liver:	n/a	chr4:143990383-143990394
24	CEBPZ	chr4:143971882-143971937	HepG2	liver:	n/a	n/a
25	CTCF	chr4:143906460-143906610	NHEK	skin:	n/a	chr4:143906543-143906559 chr4:143906542-143906560 chr4:143906544-143906565
26	CTCF	chr4:143906160-143906310	HPF	lung:	n/a	n/a
27	CTCF	chr4:144006440-144006590	NHEK	skin:	n/a	n/a
28	CTCF	chr4:143946598-143946742	GM20000	blood:	n/a	n/a
29	CTCF	chr4:143945200-143945350	GM12872	blood:	n/a	n/a
30	CTCF	chr4:143906440-143906590	Hela-S3	cervix:	n/a	chr4:143906543-143906559 chr4:143906542-143906560 chr4:143906544-143906565
31	CTCF	chr4:143906480-143906630	MCF-7	breast:	n/a	chr4:143906543-143906559 chr4:143906542-143906560 chr4:143906544-143906565
32	CTCF	chr4:143946620-143946770	HEK293	kidney:	n/a	n/a
33	CTCF	chr4:143946600-143946750	HepG2	liver:	n/a	n/a
34	CTCF	chr4:143906282-143906834	MCF-7	breast:	n/a	chr4:143906543-143906559 chr4:143906542-143906560 chr4:143906544-143906565
35	CTCF	chr4:144006526-144006696	Lung_OC	lung:	n/a	n/a
36	CTCF	chr4:144006520-144006670	AG09309	skin:	n/a	n/a
37	CTCF	chr4:143906400-143906550	GM06990	blood:	n/a	n/a
38	CTCF	chr4:143906480-143906630	BJ	skin:	n/a	chr4:143906543-143906559 chr4:143906542-143906560 chr4:143906544-143906565
39	CTCF	chr4:143906500-143906650	GM12875	blood:	n/a	chr4:143906543-143906559 chr4:143906542-143906560 chr4:143906544-143906565
40	CTCF	chr4:143946513-143946717	HepG2	liver:	n/a	n/a
41	CTCF	chr4:143906436-143906607	A549	lung:	n/a	chr4:143906543-143906559 chr4:143906542-143906560 chr4:143906544-143906565
42	CTCF	chr4:144006600-144006750	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr4:143987162-143987201	LNCaP	prostate:	n/a	n/a
44	CTCF	chr4:144006560-144006710	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr4:143946580-143946730	HFF	foreskin:	n/a	n/a
46	CTCF	chr4:143946560-143946710	HMF	breast:	n/a	n/a
47	CTCF	chr4:143906480-143906630	HRE	kidney:	n/a	chr4:143906543-143906559 chr4:143906542-143906560 chr4:143906544-143906565
48	CTCF	chr4:144006552-144006727	LNCaP	prostate:	n/a	n/a
49	CTCF	chr4:144006540-144006690	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr4:143946601-143946717	GM19240	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:143947083-143947133	HCF	heart:	n/a
2	chr4:143947083-143947133	IMR90	lung:	fetal
3	chr4:143947083-143947133	H1-hESC	embryonic stem cell:	embryo
4	chr4:143947083-143947133	Caco-2	colon:	n/a
5	chr4:143947083-143947133	BJ	skin:	n/a
6	chr4:143947083-143947133	SAEC	small airway:	n/a
7	chr4:143947083-143947133	CMK	blood:	n/a
8	chr4:143947083-143947133	MCF-7	breast:	n/a
9	chr4:143947083-143947133	K562	blood:	n/a
10	chr4:143947083-143947133	HCM	heart:	n/a
11	chr4:143947083-143947133	SK-N-SH	brain:	n/a
12	chr4:143947083-143947133	HMEC	breast:	n/a
13	chr4:143947083-143947133	HEK293	kidney:	embryo
14	chr4:143947083-143947133	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:143947083-143947133	NB4	blood:	n/a
16	chr4:143947083-143947133	HNPCEpiC	eye:	n/a
17	chr4:143947083-143947133	HCT-116	colon:	n/a
18	chr4:143947083-143947133	HUVEC	blood vessel:	n/a
19	chr4:143947083-143947133	GM12891	blood:	n/a
20	chr4:143947083-143947133	HAEpiC	amniotic membrane:	n/a
21	chr4:143947083-143947133	MCF10A-Er-Src	breast:	n/a
22	chr4:143947083-143947133	SK-N-SH_RA	brain:	n/a
23	chr4:143947083-143947133	LNCaP	prostate:	n/a
24	chr4:143947083-143947133	HL-60	blood:	n/a
25	chr4:143947083-143947133	AG09319	gingival:	n/a
26	chr4:143947083-143947133	NHBE	bronchial:	n/a
27	chr4:143947083-143947133	AG10803	skin:	n/a
28	chr4:143947083-143947133	HIPEpiC	eye:	n/a
29	chr4:143947083-143947133	BE2_C	brain:	n/a
30	chr4:143947083-143947133	AG04450	lung:	fetal
31	chr4:143947083-143947133	HCPEpiC	choroid plexus:	n/a
32	chr4:143947083-143947133	AG09309	skin:	n/a
33	chr4:143947083-143947133	AoSMC	blood vessel:	n/a
34	chr4:143947083-143947133	AG04449	skin:	fetal
35	chr4:143947083-143947133	Jurkat	blood:	n/a
36	chr4:143947083-143947133	HepG2	liver:	n/a
37	chr4:143947083-143947133	Hela-S3	cervix:	n/a
38	chr4:143947083-143947133	Hepatocyte	liver:	n/a
39	chr4:143947083-143947133	U87	brain:	n/a
40	chr4:143947083-143947133	ECC-1	luminal epithelium:	n/a
41	chr4:143947083-143947133	RPTEC	kidney:	n/a
42	chr4:143947083-143947133	GM19239	blood:	n/a
43	chr4:143947083-143947133	GM12878	blood:	n/a
44	chr4:143947083-143947133	PFSK-1	brain:	n/a
45	chr4:143947083-143947133	GM06990	blood:	n/a
46	chr4:143947083-143947133	HEEpiC	esophagus:	n/a
47	chr4:143947083-143947133	NHDF-neo	bronchial:	n/a
48	chr4:143947083-143947133	GM12892	blood:	n/a
49	chr4:143947083-143947133	HRE	kidney:	n/a
50	chr4:143947083-143947133	A549	lung:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:143920733..143921365-chr4:143957435..143958152,3	MCF-7	breast:
2	chr4:143804340..143805239-chr4:143946331..143947512,3	MCF-7	breast:
3	chr4:143998688..144000241-chr4:144017424..144020282,2	K562	blood:
4	chr20:57606842..57607490-chr4:143895238..143895857,2	MCF-7	breast:
5	chr4:143274011..143274935-chr4:143946210..143946920,2	MCF-7	breast:
6	chr4:143804603..143805356-chr4:144006149..144006825,3	MCF-7	breast:
7	chr4:143894181..143895785-chr4:143899696..143901911,2	MCF-7	breast:
8	chr4:143977110..143979922-chr4:143980152..143982987,2	K562	blood:
9	chr4:143771733..143772322-chr4:143906005..143906508,2	MCF-7	breast:
10	chr4:143977110..143979922-chr4:143980152..143982987,2	K562	blood:
11	chr4:143906143..143906667-chr4:143946471..143946983,2	MCF-7	breast:
12	chr4:144000802..144003856-chr4:144004297..144007579,3	K562	blood:
13	chr4:143894181..143895785-chr4:143899696..143901911,2	MCF-7	breast:
14	chr4:143894817..143895649-chr5:156735762..156736298,2	MCF-7	breast:
15	chr4:143905907..143906905-chr4:144005037..144005825,3	MCF-7	breast:
16	chr4:143536204..143537085-chr4:143957486..143958196,6	MCF-7	breast:
17	chr4:144002248..144004462-chr4:144004902..144006618,2	MCF-7	breast:
18	chr4:143956239..143958949-chr4:143960147..143962368,2	MCF-7	breast:
19	chr4:143941542..143943982-chr4:143948161..143949763,2	MCF-7	breast:
20	chr4:143945765..143946547-chr4:144099211..144100178,2	MCF-7	breast:
21	chr4:143768218..143770022-chr4:144005511..144007096,2	MCF-7	breast:
22	chr4:143803402..143804305-chr4:143946373..143947084,2	MCF-7	breast:
23	chr4:143941542..143943982-chr4:143948161..143949763,2	MCF-7	breast:
24	chr4:144000802..144003856-chr4:144004297..144007579,3	K562	blood:
25	chr4:143906143..143906667-chr4:143946471..143946983,2	MCF-7	breast:
26	chr4:143903053..143905362-chr4:144105356..144107537,3	MCF-7	breast:
27	chr4:143905907..143906905-chr4:144005037..144005825,3	MCF-7	breast:
28	chr4:143956239..143958949-chr4:143960147..143962368,2	MCF-7	breast:
29	chr4:143536204..143537085-chr4:143957648..143958196,3	MCF-7	breast:
30	chr4:143536310..143537064-chr4:143957404..143958197,5	MCF-7	breast:
31	chr4:144002248..144004462-chr4:144004902..144006618,2	MCF-7	breast:
32	chr4:143920733..143921365-chr4:143957435..143958152,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP38-5	chr4:143966239-143967031	NONHSAT098546

No data

Variant related genes	Relation type
ENSG00000251300	TF binding region
ENSG00000251300	CpG island
ENSG00000170185	chromatin interactions
ENSG00000250326	chromatin interactions
ENSG00000124172	chromatin interactions
ENSG00000109452	chromatin interactions

Extended variants
information (count: 2645 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2645 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573865838	chr4:143884305-143884306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs201934054	chr4:143884339-143884340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138905578	chr4:143884435-143884436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556495573	chr4:143884527-143884528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577606446	chr4:143884530-143884531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35973365	chr4:143884579-143884580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79435216	chr4:143884603-143884604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375938004	chr4:143884637-143884638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373060657	chr4:143884639-143884640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370885370	chr4:143884640-143884641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199881831	chr4:143884654-143884655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559994444	chr4:143884655-143884656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564855121	chr4:143884671-143884672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556709800	chr4:143884672-143884673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577940395	chr4:143884673-143884674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113030625	chr4:143884674-143884675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529423049	chr4:143884688-143884689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550906533	chr4:143884700-143884701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569195614	chr4:143884716-143884717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533178894	chr4:143884761-143884762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551725795	chr4:143884771-143884772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183530982	chr4:143884773-143884774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534338355	chr4:143884801-143884802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188802798	chr4:143884813-143884814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567515027	chr4:143884835-143884836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550391895	chr4:143884855-143884856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538029022	chr4:143884861-143884862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373320418	chr4:143884883-143884884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556506171	chr4:143884900-143884901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577820606	chr4:143884913-143884914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544699041	chr4:143884920-143884921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568916146	chr4:143884921-143884922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571929952	chr4:143884923-143884924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376477032	chr4:143884928-143884929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572338626	chr4:143884944-143884945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537954311	chr4:143884945-143884946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544630677	chr4:143884946-143884947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377203631	chr4:143884957-143884958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370387011	chr4:143884965-143884966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560644475	chr4:143884975-143884976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529483678	chr4:143885009-143885010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544356320	chr4:143885036-143885037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142024715	chr4:143885054-143885055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150778737	chr4:143885087-143885088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545757601	chr4:143885164-143885165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13151817	chr4:143885188-143885189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112640092	chr4:143885214-143885215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13151830	chr4:143885215-143885216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548536368	chr4:143885230-143885231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560564373	chr4:143885264-143885265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143880400-143884600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr4:143881800-143884400	Enhancers	Primary hematopoietic stem cells	blood
3	chr4:143883400-143884400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:143883400-143889200	Weak transcription	Colon Smooth Muscle	Colon
5	chr4:143883800-143884600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr4:143889200-143889800	Enhancers	Colon Smooth Muscle	Colon
7	chr4:143889800-143894200	Weak transcription	Colon Smooth Muscle	Colon
8	chr4:143890400-143890800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:143890600-143890800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr4:143894200-143895800	Enhancers	Colon Smooth Muscle	Colon
11	chr4:143894600-143894800	Enhancers	Psoas Muscle	Psoas
12	chr4:143895200-143897000	Enhancers	Rectal Smooth Muscle	rectum
13	chr4:143895600-143895800	Enhancers	Psoas Muscle	Psoas
14	chr4:143895600-143896000	Enhancers	Stomach Smooth Muscle	stomach
15	chr4:143895800-143896000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr4:143896600-143896800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr4:143899800-143900600	Enhancers	Fetal Intestine Small	intestine
18	chr4:143900200-143900600	Enhancers	Fetal Intestine Large	intestine
19	chr4:143900600-143904200	Weak transcription	Fetal Intestine Large	intestine
20	chr4:143900600-143904600	Weak transcription	Fetal Intestine Small	intestine
21	chr4:143903800-143904400	Enhancers	Fetal Lung	lung
22	chr4:143904200-143904400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:143904200-143905400	Enhancers	Fetal Intestine Large	intestine
24	chr4:143904600-143905400	Enhancers	Fetal Intestine Small	intestine
25	chr4:143905200-143905600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr4:143905200-143906800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr4:143905400-143906400	Weak transcription	Fetal Intestine Large	intestine
28	chr4:143905800-143906200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:143905800-143906400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr4:143905800-143906400	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr4:143905800-143906400	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr4:143905800-143906400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:143906000-143906400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr4:143906000-143906400	Enhancers	H1 Cell Line	embryonic stem cell
35	chr4:143906000-143906800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr4:143906400-143906600	Enhancers	Fetal Intestine Large	intestine
37	chr4:143906400-143907400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:143932800-143948000	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr4:143939800-143940000	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr4:143940000-143941600	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr4:143940600-143941400	ZNF genes & repeats	Fetal Muscle Leg	muscle
42	chr4:143940600-143941800	Weak transcription	Brain Substantia Nigra	brain
43	chr4:143941000-143942200	Enhancers	Spleen	Spleen
44	chr4:143941200-143947800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr4:143941400-143942200	Weak transcription	Fetal Muscle Leg	muscle
46	chr4:143941400-143943200	Enhancers	GM12878-XiMat	blood
47	chr4:143941600-143942400	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr4:143941600-143942400	Enhancers	Stomach Smooth Muscle	stomach
49	chr4:143941600-143944400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr4:143941800-143942200	Enhancers	Brain Substantia Nigra	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links