Variant report

Variant	esv1794809
Chromosome Location	chr3:141290177-141304631
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	ARID3A	chr3:141295781-141295788	HepG2	liver:	n/a	n/a
2	CEBPB	chr3:141295272-141295567	K562	blood:	n/a	chr3:141295399-141295412
3	CEBPB	chr3:141297080-141297471	IMR90	lung:	n/a	n/a
4	CEBPB	chr3:141297089-141297449	HepG2	liver:	n/a	n/a
5	CEBPB	chr3:141297130-141297449	A549	lung:	n/a	n/a
6	CEBPB	chr3:141297107-141297416	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr3:141295400-141295550	GM12865	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
8	CTCF	chr3:141295386-141295634	Medullo	brain:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
9	CTCF	chr3:141295440-141295590	HCPEpiC	choroid plexus:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
10	CTCF	chr3:141295460-141295610	HCT-116	colon:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
11	CTCF	chr3:141295300-141295685	GM12878	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
12	CTCF	chr3:141295500-141295650	RPTEC	kidney:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
13	CTCF	chr3:141295421-141295611	LNCaP	prostate:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
14	CTCF	chr3:141295120-141295270	BE2_C	brain:	n/a	n/a
15	CTCF	chr3:141295440-141295590	AG09319	gingival:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
16	CTCF	chr3:141295420-141295570	HBMEC	blood vessel:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
17	CTCF	chr3:141295454-141295562	GM20000	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
18	CTCF	chr3:141295461-141295563	GM13976	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
19	CTCF	chr3:141295375-141295623	Hela-S3	cervix:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
20	CTCF	chr3:141295420-141295570	HepG2	liver:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
21	CTCF	chr3:141295243-141295749	HCT-116	colon:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
22	CTCF	chr3:141295388-141295611	HepG2	liver:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
23	CTCF	chr3:141295380-141295530	HRPEpiC	eye:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
24	CTCF	chr3:141295460-141295610	GM12872	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
25	CTCF	chr3:141295240-141295390	AG09309	skin:	n/a	n/a
26	CTCF	chr3:141295440-141295590	GM12872	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
27	CTCF	chr3:141295420-141295570	GM12870	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
28	CTCF	chr3:141295400-141295550	Hela-S3	cervix:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
29	CTCF	chr3:141295380-141295530	HMEC	breast:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
30	CTCF	chr3:141295420-141295570	GM12872	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
31	CTCF	chr3:141295380-141295530	HRE	kidney:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
32	CTCF	chr3:141295373-141295631	HUVEC	blood vessel:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
33	CTCF	chr3:141295460-141295610	HAc	cerebellar:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
34	CTCF	chr3:141295398-141295599	GM12878	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
35	CTCF	chr3:141295500-141295650	Hela-S3	cervix:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
36	CTCF	chr3:141295440-141295590	BJ	skin:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
37	CTCF	chr3:141295195-141295761	HCT-116	colon:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
38	CTCF	chr3:141295400-141295550	HRE	kidney:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
39	CTCF	chr3:141295402-141295656	MCF-7	breast:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
40	CTCF	chr3:141295440-141295590	AG10803	skin:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
41	CTCF	chr3:141295380-141295530	GM12801	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
42	CTCF	chr3:141295400-141295550	GM12874	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
43	CTCF	chr3:141295420-141295570	SAEC	small airway:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
44	CTCF	chr3:141295420-141295570	GM12864	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
45	CTCF	chr3:141294913-141295848	A549	lung:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295110-141295118 chr3:141295502-141295520
46	CTCF	chr3:141295440-141295590	GM12866	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
47	CTCF	chr3:141295040-141295190	AoAF	blood vessel:	n/a	chr3:141295110-141295118
48	CTCF	chr3:141295397-141295616	LNCaP	prostate:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
49	CTCF	chr3:141295520-141295670	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr3:141295480-141295630	HCM	heart:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520

No.	Distal block	Cell Line	Cell type
1	chr3:141289820..141291967-chr3:141293825..141295688,2	MCF-7	breast:
2	chr3:141295145..141295891-chr3:141456926..141457444,2	MCF-7	breast:
3	chr3:141292412..141295097-chr3:141295843..141298423,3	K562	blood:
4	chr3:141295214..141296097-chr3:141456865..141457530,2	K562	blood:
5	chr3:141294935..141295765-chr3:141363408..141364356,4	MCF-7	breast:
6	chr3:141289287..141291021-chr3:141292681..141295308,2	MCF-7	breast:
7	chr3:141295275..141295993-chr3:141593960..141594866,2	MCF-7	breast:
8	chr3:141289820..141291967-chr3:141293825..141295688,2	MCF-7	breast:
9	chr3:141289287..141291021-chr3:141292681..141295308,2	MCF-7	breast:
10	chr3:141287617..141290241-chr3:141292513..141294840,2	K562	blood:
11	chr3:141279547..141282126-chr3:141289816..141292776,2	K562	blood:
12	chr3:141291433..141293078-chr3:141457049..141459142,2	MCF-7	breast:
13	chr3:141296186..141298105-chr3:141594416..141596281,2	MCF-7	breast:
14	chr3:141300234..141304209-chr3:141304484..141307292,3	K562	blood:
15	chr3:141287617..141290241-chr3:141292513..141294840,2	K562	blood:
16	chr3:141301255..141303348-chr3:141304484..141306146,2	K562	blood:
17	chr3:141299643..141301843-chr3:141308468..141311186,2	MCF-7	breast:
18	chr3:141205878..141208438-chr3:141299317..141301173,2	K562	blood:
19	chr3:141295052..141295995-chr3:141363331..141364146,2	MCF-7	breast:
20	chr3:141173922..141177182-chr3:141288723..141292910,3	MCF-7	breast:
21	chr3:141296069..141298248-chr3:141594604..141596170,2	K562	blood:
22	chr3:141303655..141305164-chr3:141310837..141312701,2	K562	blood:
23	chr3:141205222..141206757-chr3:141290019..141291835,2	K562	blood:
24	chr3:141000930..141002501-chr3:141293837..141295898,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZBTB38-5	chr3:141298279-141298331	NONHSAT092436
2	lnc-ZBTB38-5	chr3:141297366-141297596	NONHSAT092436
3	lnc-ZBTB38-5	chr3:141299210-141299287	NONHSAT092436

Variant related genes	Relation type
RASA2	TF binding region
ENSG00000069849	chromatin interactions
ENSG00000114125	chromatin interactions
ENSG00000155903	chromatin interactions

Extended variants
information (count: 496 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367737997	chr3:141290202-141290203	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs200351819	chr3:141290222-141290223	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs369313992	chr3:141290230-141290231	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs372916137	chr3:141290251-141290252	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553410356	chr3:141290258-141290259	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376949728	chr3:141290291-141290292	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs369032376	chr3:141290306-141290307	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs61740789	chr3:141290369-141290370	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs150714336	chr3:141290445-141290446	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs572955506	chr3:141290462-141290463	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs534040466	chr3:141290569-141290570	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs78074823	chr3:141290584-141290585	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs368775723	chr3:141290602-141290603	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113631794	chr3:141290616-141290617	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188171367	chr3:141290628-141290629	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563221453	chr3:141290630-141290631	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575022485	chr3:141290650-141290651	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs191129705	chr3:141290728-141290729	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560523110	chr3:141290771-141290772	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs527854515	chr3:141290777-141290778	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs139047631	chr3:141290778-141290779	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564620654	chr3:141290781-141290782	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532006956	chr3:141290807-141290808	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs550159870	chr3:141290819-141290820	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs72039522	chr3:141290872-141290873	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs10530811	chr3:141290881-141290882	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs71837437	chr3:141290884-141290885	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs57852582	chr3:141290893-141290894	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201718463	chr3:141290901-141290902	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs4683611	chr3:141290903-141290904	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
31	rs374643522	chr3:141290904-141290905	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs6804207	chr3:141290905-141290906	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs60158029	chr3:141290907-141290908	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs577484379	chr3:141290921-141290922	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs548420718	chr3:141290942-141290943	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs367892186	chr3:141290964-141290965	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371467254	chr3:141291060-141291061	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs562971042	chr3:141291172-141291173	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs149476319	chr3:141291186-141291187	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs9819771	chr3:141291187-141291188	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs111745939	chr3:141291218-141291219	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs577392479	chr3:141291219-141291220	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs538281344	chr3:141291315-141291316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs147167132	chr3:141291330-141291331	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs188741129	chr3:141291379-141291380	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181208295	chr3:141291416-141291417	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs146956359	chr3:141291497-141291498	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs376529386	chr3:141291591-141291592	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs41265465	chr3:141291628-141291629	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs112697781	chr3:141291652-141291653	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21785460	CNVD

Chromatin state (count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141236400-141301000	Weak transcription	Brain Substantia Nigra	brain
2	chr3:141236400-141306600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr3:141236600-141297000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr3:141236600-141299400	Weak transcription	Gastric	stomach
5	chr3:141237000-141299400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr3:141243400-141299400	Weak transcription	Spleen	Spleen
7	chr3:141254600-141294400	Weak transcription	Esophagus	oesophagus
8	chr3:141254800-141291400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr3:141254800-141292200	Weak transcription	Left Ventricle	heart
10	chr3:141254800-141295200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr3:141254800-141299200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr3:141254800-141299400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr3:141254800-141299400	Weak transcription	Right Ventricle	heart
14	chr3:141254800-141319200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr3:141255200-141304800	Weak transcription	Ovary	ovary
16	chr3:141255200-141320000	Weak transcription	Brain Cingulate Gyrus	brain
17	chr3:141255400-141319200	Weak transcription	Aorta	Aorta
18	chr3:141257000-141300200	Weak transcription	Pancreas	Pancrea
19	chr3:141263600-141292000	Weak transcription	Colonic Mucosa	Colon
20	chr3:141265000-141290200	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr3:141265200-141336200	Weak transcription	Psoas Muscle	Psoas
22	chr3:141267000-141290200	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr3:141267400-141295000	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr3:141268400-141297800	Weak transcription	Fetal Heart	heart
25	chr3:141269200-141294400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr3:141271200-141299400	Weak transcription	Brain Angular Gyrus	brain
27	chr3:141272400-141291400	Weak transcription	GM12878-XiMat	blood
28	chr3:141272600-141319200	Strong transcription	Dnd41	blood
29	chr3:141275800-141320600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr3:141276000-141290400	Weak transcription	Brain Germinal Matrix	brain
31	chr3:141276000-141299400	Weak transcription	Rectal Smooth Muscle	rectum
32	chr3:141276200-141290200	Weak transcription	Fetal Muscle Trunk	muscle
33	chr3:141276200-141291000	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr3:141276200-141291200	Weak transcription	Brain Hippocampus Middle	brain
35	chr3:141276200-141291200	Weak transcription	Fetal Muscle Leg	muscle
36	chr3:141276200-141291400	Weak transcription	Fetal Brain Female	brain
37	chr3:141276200-141297000	Weak transcription	Lung	lung
38	chr3:141276400-141329400	Weak transcription	Small Intestine	intestine
39	chr3:141276600-141290400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr3:141276600-141291400	Weak transcription	Fetal Lung	lung
41	chr3:141276600-141292200	Weak transcription	HSMMtube	muscle
42	chr3:141277200-141297000	Weak transcription	Thymus	Thymus
43	chr3:141277200-141341400	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr3:141277400-141293600	Weak transcription	Fetal Kidney	kidney
45	chr3:141277600-141296400	Weak transcription	Hela-S3	cervix
46	chr3:141277800-141312000	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr3:141278000-141296800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr3:141279200-141292200	Weak transcription	NHLF	lung
49	chr3:141280000-141290200	Weak transcription	NH-A	brain
50	chr3:141280200-141290600	Weak transcription	Duodenum Smooth Muscle	Duodenum

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