Variant report

Variant	esv1795799
Chromosome Location	chr3:141284383-141301451
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	chr3:141297107-141297416	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr3:141297089-141297449	HepG2	liver:	n/a	n/a
4	CEBPB	chr3:141297130-141297449	A549	lung:	n/a	n/a
5	CEBPB	chr3:141295272-141295567	K562	blood:	n/a	chr3:141295399-141295412
6	CEBPB	chr3:141297080-141297471	IMR90	lung:	n/a	n/a
7	CEBPB	chr3:141288447-141288647	K562	blood:	n/a	n/a
8	CTCF	chr3:141295406-141295569	SK-N-SH_RA	brain:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
9	CTCF	chr3:141295375-141295623	Hela-S3	cervix:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
10	CTCF	chr3:141295440-141295590	HUVEC	blood vessel:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
11	CTCF	chr3:141295440-141295590	HCPEpiC	choroid plexus:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
12	CTCF	chr3:141295360-141295510	GM12868	blood:	n/a	n/a
13	CTCF	chr3:141295411-141295585	GM10266	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
14	CTCF	chr3:141295400-141295550	GM12874	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
15	CTCF	chr3:141295320-141295470	BE2_C	brain:	n/a	n/a
16	CTCF	chr3:141295460-141295610	HVMF	connective:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
17	CTCF	chr3:141295440-141295590	SK-N-SH_RA	brain:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
18	CTCF	chr3:141295420-141295570	HPF	lung:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
19	CTCF	chr3:141295400-141295550	SK-N-SH_RA	brain:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
20	CTCF	chr3:141295380-141295530	HCT-116	colon:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
21	CTCF	chr3:141295400-141295550	HEEpiC	esophagus:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
22	CTCF	chr3:141295420-141295570	BJ	skin:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
23	CTCF	chr3:141295440-141295590	HA-sp	spinal cord:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
24	CTCF	chr3:141295440-141295590	NHDF-neo	bronchial:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
25	CTCF	chr3:141295380-141295530	GM12867	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
26	CTCF	chr3:141295420-141295570	GM06990	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
27	CTCF	chr3:141295407-141295588	Pancreas_OC	pancreas:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
28	CTCF	chr3:141295440-141295590	BJ	skin:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
29	CTCF	chr3:141295398-141295620	K562	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
30	CTCF	chr3:141295373-141295631	HUVEC	blood vessel:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
31	CTCF	chr3:141295380-141295530	HVMF	connective:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
32	CTCF	chr3:141295416-141295605	H1-hESC	embryonic stem cell:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
33	CTCF	chr3:141295284-141295707	T-47D	breast:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
34	CTCF	chr3:141295397-141295616	LNCaP	prostate:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
35	CTCF	chr3:141295420-141295570	AG04449	skin:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
36	CTCF	chr3:141295420-141295570	GM12872	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
37	CTCF	chr3:141294913-141295848	A549	lung:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295110-141295118 chr3:141295502-141295520
38	CTCF	chr3:141295454-141295562	GM20000	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
39	CTCF	chr3:141295400-141295550	Hela-S3	cervix:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
40	CTCF	chr3:141286141-141286190	GM20000	blood:	n/a	n/a
41	CTCF	chr3:141295420-141295570	HMEC	breast:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
42	CTCF	chr3:141295420-141295570	HRPEpiC	eye:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
43	CTCF	chr3:141295440-141295590	WERI-Rb-1	eye:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
44	CTCF	chr3:141295400-141295550	HMF	breast:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
45	CTCF	chr3:141295460-141295610	MCF-7	breast:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
46	CTCF	chr3:141295020-141295170	HMEC	breast:	n/a	chr3:141295110-141295118
47	CTCF	chr3:141295400-141295550	HUVEC	blood vessel:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
48	CTCF	chr3:141295460-141295610	GM12873	blood:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
49	CTCF	chr3:141295421-141295611	LNCaP	prostate:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520
50	CTCF	chr3:141295386-141295634	Medullo	brain:	n/a	chr3:141295504-141295525 chr3:141295506-141295513 chr3:141295502-141295520

No.	Distal block	Cell Line	Cell type
1	chr3:141205878..141208438-chr3:141299317..141301173,2	K562	blood:
2	chr3:141291433..141293078-chr3:141457049..141459142,2	MCF-7	breast:
3	chr3:141301255..141303348-chr3:141304484..141306146,2	K562	blood:
4	chr3:141204998..141206797-chr3:141284202..141286534,3	K562	blood:
5	chr3:141279547..141282126-chr3:141289816..141292776,2	K562	blood:
6	chr3:141295052..141295995-chr3:141363331..141364146,2	MCF-7	breast:
7	chr3:141294935..141295765-chr3:141363408..141364356,4	MCF-7	breast:
8	chr3:141289287..141291021-chr3:141292681..141295308,2	MCF-7	breast:
9	chr3:141205222..141206757-chr3:141290019..141291835,2	K562	blood:
10	chr3:141287617..141290241-chr3:141292513..141294840,2	K562	blood:
11	chr3:141296069..141298248-chr3:141594604..141596170,2	K562	blood:
12	chr3:141173922..141177182-chr3:141288723..141292910,3	MCF-7	breast:
13	chr3:141295145..141295891-chr3:141456926..141457444,2	MCF-7	breast:
14	chr3:141282988..141284953-chr3:141284955..141286528,2	MCF-7	breast:
15	chr3:141287617..141290241-chr3:141292513..141294840,2	K562	blood:
16	chr3:141296186..141298105-chr3:141594416..141596281,2	MCF-7	breast:
17	chr3:141282047..141283731-chr3:141285976..141288071,2	K562	blood:
18	chr3:141300234..141304209-chr3:141304484..141307292,3	K562	blood:
19	chr3:141286560..141289498-chr3:141377973..141379933,2	MCF-7	breast:
20	chr3:141289820..141291967-chr3:141293825..141295688,2	MCF-7	breast:
21	chr3:141299643..141301843-chr3:141308468..141311186,2	MCF-7	breast:
22	chr3:141292412..141295097-chr3:141295843..141298423,3	K562	blood:
23	chr3:141295275..141295993-chr3:141593960..141594866,2	MCF-7	breast:
24	chr3:141000930..141002501-chr3:141293837..141295898,2	K562	blood:
25	chr3:141289820..141291967-chr3:141293825..141295688,2	MCF-7	breast:
26	chr3:141028943..141030664-chr3:141287005..141289345,2	MCF-7	breast:
27	chr3:141289287..141291021-chr3:141292681..141295308,2	MCF-7	breast:
28	chr3:141282988..141284953-chr3:141284955..141286528,2	MCF-7	breast:
29	chr3:141287028..141289091-chr3:141363871..141366477,2	K562	blood:
30	chr3:141295214..141296097-chr3:141456865..141457530,2	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: 549 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12695740	chr3:141284383-141284384	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs113176107	chr3:141284407-141284408	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs568261777	chr3:141284439-141284440	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs529059676	chr3:141284473-141284474	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs547593213	chr3:141284478-141284479	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566150384	chr3:141284499-141284500	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539480314	chr3:141284525-141284526	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs113479059	chr3:141284569-141284570	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs59162381	chr3:141284659-141284660	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs111909082	chr3:141284694-141284695	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555594472	chr3:141284717-141284718	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs74454986	chr3:141284719-141284720	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs568427476	chr3:141284753-141284754	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs187517983	chr3:141284777-141284778	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553612982	chr3:141284873-141284874	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs112899713	chr3:141284905-141284906	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs551260116	chr3:141285017-141285018	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs80255756	chr3:141285060-141285061	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs373211881	chr3:141285088-141285089	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540524162	chr3:141285136-141285137	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs117283527	chr3:141285174-141285175	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs78175746	chr3:141285182-141285183	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375130630	chr3:141285196-141285197	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs79680093	chr3:141285224-141285225	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557281621	chr3:141285306-141285307	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs185126106	chr3:141285316-141285317	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs190821846	chr3:141285337-141285338	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560627387	chr3:141285344-141285345	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs182012099	chr3:141285362-141285363	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576995536	chr3:141285402-141285403	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533457744	chr3:141285439-141285440	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs551422305	chr3:141285605-141285606	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs569719781	chr3:141285612-141285613	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537012072	chr3:141285617-141285618	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184618361	chr3:141285655-141285656	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs567926064	chr3:141285700-141285701	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529249256	chr3:141285780-141285781	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs12695741	chr3:141285783-141285784	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs199974617	chr3:141285794-141285795	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs578078943	chr3:141285865-141285866	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs188021047	chr3:141285879-141285880	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181270581	chr3:141285988-141285989	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576125645	chr3:141286007-141286008	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371822168	chr3:141286013-141286014	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373953844	chr3:141286081-141286082	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543428573	chr3:141286104-141286105	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185288930	chr3:141286130-141286131	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs369516554	chr3:141286140-141286141	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs142581242	chr3:141286150-141286151	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573879003	chr3:141286172-141286173	Weak transcription Strong transcription	Chromatin interactive region	1 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:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr3:141263800-141288800	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr3:141265000-141290200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr3:141265200-141336200	Weak transcription	Psoas Muscle	Psoas
23	chr3:141267000-141289400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:141267000-141290200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr3:141267400-141295000	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr3:141268400-141297800	Weak transcription	Fetal Heart	heart
27	chr3:141269200-141294400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr3:141271200-141299400	Weak transcription	Brain Angular Gyrus	brain
29	chr3:141272400-141291400	Weak transcription	GM12878-XiMat	blood
30	chr3:141272600-141319200	Strong transcription	Dnd41	blood
31	chr3:141272800-141285800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr3:141275800-141320600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr3:141276000-141290400	Weak transcription	Brain Germinal Matrix	brain
34	chr3:141276000-141299400	Weak transcription	Rectal Smooth Muscle	rectum
35	chr3:141276200-141289400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr3:141276200-141289800	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr3:141276200-141290200	Weak transcription	Fetal Muscle Trunk	muscle
38	chr3:141276200-141291000	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr3:141276200-141291200	Weak transcription	Brain Hippocampus Middle	brain
40	chr3:141276200-141291200	Weak transcription	Fetal Muscle Leg	muscle
41	chr3:141276200-141291400	Weak transcription	Fetal Brain Female	brain
42	chr3:141276200-141297000	Weak transcription	Lung	lung
43	chr3:141276400-141288600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:141276400-141329400	Weak transcription	Small Intestine	intestine
45	chr3:141276600-141290400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr3:141276600-141291400	Weak transcription	Fetal Lung	lung
47	chr3:141276600-141292200	Weak transcription	HSMMtube	muscle
48	chr3:141277200-141297000	Weak transcription	Thymus	Thymus
49	chr3:141277200-141341400	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr3:141277400-141293600	Weak transcription	Fetal Kidney	kidney

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links