Variant report

Variant	nsv880176
Chromosome Location	chr4:143929235-144027729
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:473)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:143946228-143946800	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr4:143946252-143946526	GM12878	blood:	n/a	chr4:143946422-143946433
3	BATF	chr4:143942530-143942886	GM12878	blood:	n/a	n/a
4	BATF	chr4:143942531-143942863	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:143994101-143994135	K562	blood:	n/a	n/a
6	CEBPB	chr4:144003941-144004242	A549	lung:	n/a	n/a
7	CEBPB	chr4:143947235-143947385	A549	lung:	n/a	chr4:143947312-143947323
8	CEBPB	chr4:143944806-143945035	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr4:143990215-143990486	K562	blood:	n/a	chr4:143990383-143990394
10	CEBPB	chr4:143990213-143990556	HepG2	liver:	n/a	chr4:143990383-143990394
11	CEBPB	chr4:143944802-143945077	A549	lung:	n/a	n/a
12	CEBPB	chr4:143957621-143957929	MCF-7	breast:	n/a	n/a
13	CEBPB	chr4:144004785-144005093	Hela-S3	cervix:	n/a	chr4:144004855-144004872
14	CEBPB	chr4:144013004-144013355	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:144010523-144010781	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr4:143947157-143947447	HepG2	liver:	n/a	chr4:143947312-143947323
17	CEBPB	chr4:143984737-143984932	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:144003938-144004253	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:143990289-143990526	IMR90	lung:	n/a	chr4:143990383-143990394
20	CEBPB	chr4:143984634-143984998	HCT-116	colon:	n/a	n/a
21	CEBPZ	chr4:143971882-143971937	HepG2	liver:	n/a	n/a
22	CTCF	chr4:143946480-143946756	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr4:143946598-143946742	GM20000	blood:	n/a	n/a
24	CTCF	chr4:143946601-143946717	GM19240	blood:	n/a	n/a
25	CTCF	chr4:143946551-143946714	A549	lung:	n/a	n/a
26	CTCF	chr4:143941680-143941830	MCF-7	breast:	n/a	n/a
27	CTCF	chr4:144006500-144006650	AG09319	gingival:	n/a	n/a
28	CTCF	chr4:143946500-143946650	WI-38	lung:	n/a	n/a
29	CTCF	chr4:143941680-143941830	GM12866	blood:	n/a	n/a
30	CTCF	chr4:144005471-144005512	LNCaP	prostate:	n/a	n/a
31	CTCF	chr4:143946600-143946750	AG04449	skin:	n/a	n/a
32	CTCF	chr4:143946620-143946770	GM12867	blood:	n/a	n/a
33	CTCF	chr4:143946576-143946729	HepG2	liver:	n/a	n/a
34	CTCF	chr4:144006529-144006717	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr4:144006500-144006650	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr4:143946580-143946730	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr4:143941540-143941690	GM12872	blood:	n/a	n/a
38	CTCF	chr4:143946559-143946758	A549	lung:	n/a	n/a
39	CTCF	chr4:144006580-144006730	AG10803	skin:	n/a	n/a
40	CTCF	chr4:143946615-143946723	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr4:144006440-144006590	HFF	foreskin:	n/a	n/a
42	CTCF	chr4:144006660-144006810	GM06990	blood:	n/a	n/a
43	CTCF	chr4:143941680-143941830	HEK293	kidney:	n/a	n/a
44	CTCF	chr4:144006520-144006670	AG09309	skin:	n/a	n/a
45	CTCF	chr4:143946500-143946650	HRE	kidney:	n/a	n/a
46	CTCF	chr4:143946550-143946783	GM12878	blood:	n/a	n/a
47	CTCF	chr4:143941680-143941830	GM12875	blood:	n/a	n/a
48	CTCF	chr4:143946597-143946759	GM13977	blood:	n/a	n/a
49	CTCF	chr4:143946289-143946948	SK-N-SH	brain:	n/a	n/a
50	CTCF	chr4:143946780-143946930	HAc	cerebellar:	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	MCF-7	breast:	n/a
2	chr4:143947083-143947133	Jurkat	blood:	n/a
3	chr4:143947083-143947133	PANC-1	pancreas:	n/a
4	chr4:143947083-143947133	NHBE	bronchial:	n/a
5	chr4:143947083-143947133	NHDF-neo	bronchial:	n/a
6	chr4:143947083-143947133	HIPEpiC	eye:	n/a
7	chr4:143947083-143947133	ovcar-3	ovarian:	n/a
8	chr4:143947083-143947133	AoSMC	blood vessel:	n/a
9	chr4:143947083-143947133	ProgFib	skin:	n/a
10	chr4:143947083-143947133	LNCaP	prostate:	n/a
11	chr4:143947083-143947133	Caco-2	colon:	n/a
12	chr4:143947083-143947133	PrEC	prostate:	n/a
13	chr4:143947083-143947133	K562	blood:	n/a
14	chr4:143947083-143947133	Hepatocyte	liver:	n/a
15	chr4:143947083-143947133	HEK293	kidney:	embryo
16	chr4:143947083-143947133	HMEC	breast:	n/a
17	chr4:143947083-143947133	T-47D	breast:	n/a
18	chr4:143947083-143947133	MCF10A-Er-Src	breast:	n/a
19	chr4:143947083-143947133	GM19239	blood:	n/a
20	chr4:143947083-143947133	AG09319	gingival:	n/a
21	chr4:143947083-143947133	HCT-116	colon:	n/a
22	chr4:143947083-143947133	ECC-1	luminal epithelium:	n/a
23	chr4:143947083-143947133	HRCEpiC	kidney:	n/a
24	chr4:143947083-143947133	CMK	blood:	n/a
25	chr4:143947083-143947133	NB4	blood:	n/a
26	chr4:143947083-143947133	A549	lung:	n/a
27	chr4:143947083-143947133	U87	brain:	n/a
28	chr4:143947083-143947133	PFSK-1	brain:	n/a
29	chr4:143947083-143947133	HRE	kidney:	n/a
30	chr4:143947083-143947133	AG10803	skin:	n/a
31	chr4:143947083-143947133	SK-N-SH	brain:	n/a
32	chr4:143947083-143947133	HCPEpiC	choroid plexus:	n/a
33	chr4:143947083-143947133	BE2_C	brain:	n/a
34	chr4:143947083-143947133	GM12892	blood:	n/a
35	chr4:143947083-143947133	H1-hESC	embryonic stem cell:	embryo
36	chr4:143947083-143947133	NH-A	brain:	n/a
37	chr4:143947083-143947133	SKMC	muscle:	n/a
38	chr4:143947083-143947133	NT2-D1	testis:	n/a
39	chr4:143947083-143947133	SK-N-MC	brain:	n/a
40	chr4:143947083-143947133	GM12878	blood:	n/a
41	chr4:143947083-143947133	SAEC	small airway:	n/a
42	chr4:143947083-143947133	BJ	skin:	n/a
43	chr4:143947083-143947133	HCM	heart:	n/a
44	chr4:143947083-143947133	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:143947083-143947133	HRPEpiC	eye:	n/a
46	chr4:143947083-143947133	HEEpiC	esophagus:	n/a
47	chr4:143947083-143947133	RPTEC	kidney:	n/a
48	chr4:143947083-143947133	SK-N-SH_RA	brain:	n/a
49	chr4:143947083-143947133	GM06990	blood:	n/a
50	chr4:143947083-143947133	HCF	heart:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:143956239..143958949-chr4:143960147..143962368,2	MCF-7	breast:
2	chr4:143998688..144000241-chr4:144017424..144020282,2	K562	blood:
3	chr4:143536310..143537064-chr4:143957404..143958197,5	MCF-7	breast:
4	chr4:143536204..143537085-chr4:143957648..143958196,3	MCF-7	breast:
5	chr4:143977110..143979922-chr4:143980152..143982987,2	K562	blood:
6	chr4:143536204..143537085-chr4:143957486..143958196,6	MCF-7	breast:
7	chr4:144000802..144003856-chr4:144004297..144007579,3	K562	blood:
8	chr4:143905907..143906905-chr4:144005037..144005825,3	MCF-7	breast:
9	chr4:144000802..144003856-chr4:144004297..144007579,3	K562	blood:
10	chr4:143977110..143979922-chr4:143980152..143982987,2	K562	blood:
11	chr4:143274011..143274935-chr4:143946210..143946920,2	MCF-7	breast:
12	chr4:144027503..144029840-chr4:144031785..144033954,2	K562	blood:
13	chr4:144002248..144004462-chr4:144004902..144006618,2	MCF-7	breast:
14	chr4:144002248..144004462-chr4:144004902..144006618,2	MCF-7	breast:
15	chr4:143804340..143805239-chr4:143946331..143947512,3	MCF-7	breast:
16	chr4:143945765..143946547-chr4:144099211..144100178,2	MCF-7	breast:
17	chr4:143803402..143804305-chr4:143946373..143947084,2	MCF-7	breast:
18	chr4:143906143..143906667-chr4:143946471..143946983,2	MCF-7	breast:
19	chr4:143920733..143921365-chr4:143957435..143958152,3	MCF-7	breast:
20	chr4:143998688..144000241-chr4:144017424..144020282,2	K562	blood:
21	chr4:143956239..143958949-chr4:143960147..143962368,2	MCF-7	breast:
22	chr4:143804603..143805356-chr4:144006149..144006825,3	MCF-7	breast:
23	chr4:143768218..143770022-chr4:144005511..144007096,2	MCF-7	breast:
24	chr4:143941542..143943982-chr4:143948161..143949763,2	MCF-7	breast:
25	chr4:143941542..143943982-chr4:143948161..143949763,2	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
ENSG00000109452	chromatin interactions

Extended variants
information (count: 2285 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2285 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376708590	chr4:143932820-143932821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182940793	chr4:143932839-143932840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532559323	chr4:143932904-143932905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554103593	chr4:143932968-143932969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548411099	chr4:143932988-143932989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533206817	chr4:143933059-143933060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567285268	chr4:143933079-143933080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34308722	chr4:143933089-143933090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370045106	chr4:143933125-143933126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551729901	chr4:143933128-143933129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs955722	chr4:143933140-143933141	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs113248619	chr4:143933166-143933167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375446609	chr4:143933261-143933262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551058337	chr4:143933328-143933329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567077934	chr4:143933377-143933378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537773785	chr4:143933392-143933393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185360384	chr4:143933394-143933395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577490305	chr4:143933424-143933425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376474192	chr4:143933452-143933453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540373960	chr4:143933456-143933457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544723445	chr4:143933474-143933475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575142351	chr4:143933535-143933536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553717063	chr4:143933571-143933572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572054788	chr4:143933591-143933592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368924636	chr4:143933602-143933603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542658614	chr4:143933604-143933605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562289924	chr4:143933613-143933614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574250419	chr4:143933614-143933615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544804313	chr4:143933623-143933624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190216791	chr4:143933635-143933636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182150914	chr4:143933656-143933657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs60649154	chr4:143933825-143933826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373932015	chr4:143933857-143933858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187738415	chr4:143933863-143933864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560499572	chr4:143933891-143933892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527787856	chr4:143933894-143933895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549040446	chr4:143933912-143933913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373160748	chr4:143933979-143933980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567142856	chr4:143934047-143934048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61741556	chr4:143934060-143934061	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs549559061	chr4:143934075-143934076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61740259	chr4:143934106-143934107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369591732	chr4:143934113-143934114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6821582	chr4:143934141-143934142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs553490307	chr4:143934167-143934168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571978465	chr4:143934215-143934216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs193250269	chr4:143934271-143934272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572832548	chr4:143934357-143934358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13115992	chr4:143934410-143934411	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs576184977	chr4:143934414-143934415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143932800-143948000	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr4:143939800-143940000	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr4:143940000-143941600	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr4:143940600-143941400	ZNF genes & repeats	Fetal Muscle Leg	muscle
5	chr4:143940600-143941800	Weak transcription	Brain Substantia Nigra	brain
6	chr4:143941000-143942200	Enhancers	Spleen	Spleen
7	chr4:143941200-143947800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr4:143941400-143942200	Weak transcription	Fetal Muscle Leg	muscle
9	chr4:143941400-143943200	Enhancers	GM12878-XiMat	blood
10	chr4:143941600-143942400	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr4:143941600-143942400	Enhancers	Stomach Smooth Muscle	stomach
12	chr4:143941600-143944400	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr4:143941800-143942200	Enhancers	Brain Substantia Nigra	brain
14	chr4:143941800-143942600	Enhancers	Primary B cells from peripheral blood	blood
15	chr4:143942000-143942600	Enhancers	Adipose Nuclei	Adipose
16	chr4:143942200-143942400	Enhancers	Fetal Muscle Leg	muscle
17	chr4:143942200-143942600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr4:143942200-143942600	Enhancers	Fetal Stomach	stomach
19	chr4:143942200-143944400	Weak transcription	Spleen	Spleen
20	chr4:143942600-143946800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr4:143943200-143944400	Weak transcription	GM12878-XiMat	blood
22	chr4:143944400-143944600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:143944400-143944600	Enhancers	Spleen	Spleen
24	chr4:143944400-143944800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr4:143944400-143944800	Enhancers	GM12878-XiMat	blood
26	chr4:143944400-143945000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr4:143944400-143945200	Enhancers	Muscle Satellite Cultured Cells	--
28	chr4:143944600-143945400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:143944800-143946200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr4:143945000-143945600	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr4:143945200-143946200	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr4:143945200-143946800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr4:143945400-143946600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:143945600-143946800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr4:143946000-143946600	Enhancers	Osteobl	bone
36	chr4:143946200-143946400	Enhancers	Esophagus	oesophagus
37	chr4:143946200-143946600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr4:143946200-143946600	Enhancers	Primary hematopoietic stem cells	blood
39	chr4:143946200-143946600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:143946200-143946600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr4:143946200-143946800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr4:143946200-143947000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr4:143946200-143947000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr4:143946200-143947000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr4:143946200-143948200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:143946400-143946600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr4:143946400-143946600	Enhancers	A549	lung
48	chr4:143946400-143947400	Weak transcription	Esophagus	oesophagus
49	chr4:143946600-143947600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr4:143946600-143947800	Weak transcription	Muscle Satellite Cultured Cells	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links