Variant report

Variant	nsv984450
Chromosome Location	chr2:96936273-96951139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:441)
CpG islands
(count:245)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr2:96938414-96938919	A549	lung:	n/a	n/a
2	BCL3	chr2:96937672-96938313	A549	lung:	n/a	n/a
3	BHLHE40	chr2:96937930-96937972	K562	blood:	n/a	n/a
4	BRCA1	chr2:96940979-96941127	Hela-S3	cervix:	n/a	n/a
5	CCNT2	chr2:96940111-96940430	K562	blood:	n/a	n/a
6	CTCF	chr2:96937840-96937990	WERI-Rb-1	eye:	n/a	n/a
7	CTCF	chr2:96937820-96937970	HPF	lung:	n/a	n/a
8	CTCF	chr2:96937860-96938010	GM12873	blood:	n/a	n/a
9	CTCF	chr2:96937820-96937970	Caco-2	colon:	n/a	n/a
10	CTCF	chr2:96937920-96938070	NB4	blood:	n/a	n/a
11	CTCF	chr2:96937840-96937990	AG09319	gingival:	n/a	n/a
12	CTCF	chr2:96937900-96938050	NHDF-neo	bronchial:	n/a	n/a
13	CTCF	chr2:96937886-96937995	MCF-7	breast:	n/a	n/a
14	CTCF	chr2:96937880-96938030	HVMF	connective:	n/a	n/a
15	CTCF	chr2:96937840-96937990	AG10803	skin:	n/a	n/a
16	CTCF	chr2:96937920-96938070	HPF	lung:	n/a	n/a
17	CTCF	chr2:96937868-96938007	GM12878	blood:	n/a	n/a
18	CTCF	chr2:96937900-96938050	AG04449	skin:	n/a	n/a
19	CTCF	chr2:96937980-96938130	BJ	skin:	n/a	n/a
20	CTCF	chr2:96937800-96937950	HCM	heart:	n/a	n/a
21	CTCF	chr2:96937880-96938030	GM12873	blood:	n/a	n/a
22	CTCF	chr2:96937868-96938021	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr2:96937880-96938030	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr2:96937820-96937970	MCF-7	breast:	n/a	n/a
25	CTCF	chr2:96937840-96937990	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr2:96937860-96938010	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr2:96937886-96937997	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr2:96937860-96938010	MCF-7	breast:	n/a	n/a
29	CTCF	chr2:96937854-96938003	K562	blood:	n/a	n/a
30	CTCF	chr2:96937771-96938059	HepG2	liver:	n/a	n/a
31	CTCF	chr2:96938100-96938250	Caco-2	colon:	n/a	n/a
32	CTCF	chr2:96937893-96937975	GM12892	blood:	n/a	n/a
33	CTCF	chr2:96937874-96938021	HepG2	liver:	n/a	n/a
34	CTCF	chr2:96937890-96938005	GM10266	blood:	n/a	n/a
35	CTCF	chr2:96937843-96938024	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:96937920-96938070	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr2:96937790-96938039	HepG2	liver:	n/a	n/a
38	CTCF	chr2:96937840-96937990	Caco-2	colon:	n/a	n/a
39	CTCF	chr2:96937880-96938030	HepG2	liver:	n/a	n/a
40	CTCF	chr2:96937750-96938064	K562	blood:	n/a	n/a
41	CTCF	chr2:96937980-96938130	HMEC	breast:	n/a	n/a
42	CTCF	chr2:96937860-96938010	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr2:96937760-96937910	SAEC	small airway:	n/a	n/a
44	CTCF	chr2:96937931-96937973	GM10248	blood:	n/a	n/a
45	CTCF	chr2:96937899-96937999	Gliobla	brain:	n/a	n/a
46	CTCF	chr2:96937860-96938010	GM12865	blood:	n/a	n/a
47	CTCF	chr2:96937757-96938107	GM12878	blood:	n/a	n/a
48	CTCF	chr2:96937820-96937970	K562	blood:	n/a	n/a
49	CTCF	chr2:96937900-96938050	GM12870	blood:	n/a	n/a
50	CTCF	chr2:96937940-96938090	HFF-Myc	foreskin:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96940284-96940334	U87	brain:	n/a
2	chr2:96940284-96940334	U87	brain:	n/a
3	chr2:96937097-96937147	HIPEpiC	eye:	n/a
4	chr2:96944360-96944410	SAEC	small airway:	n/a
5	chr2:96940284-96940334	HNPCEpiC	eye:	n/a
6	chr2:96944360-96944410	IMR90	lung:	fetal
7	chr2:96944236-96944286	HCM	heart:	n/a
8	chr2:96940284-96940334	HRE	kidney:	n/a
9	chr2:96944236-96944286	RPTEC	kidney:	n/a
10	chr2:96937097-96937147	NT2-D1	testis:	n/a
11	chr2:96940284-96940334	BJ	skin:	n/a
12	chr2:96937097-96937147	HRPEpiC	eye:	n/a
13	chr2:96940284-96940334	Hela-S3	cervix:	n/a
14	chr2:96944236-96944286	HIPEpiC	eye:	n/a
15	chr2:96937097-96937147	H1-hESC	embryonic stem cell:	embryo
16	chr2:96944236-96944286	U87	brain:	n/a
17	chr2:96944236-96944286	AG09309	skin:	n/a
18	chr2:96944236-96944286	AoSMC	blood vessel:	n/a
19	chr2:96944236-96944286	PFSK-1	brain:	n/a
20	chr2:96940284-96940334	NHDF-neo	bronchial:	n/a
21	chr2:96940284-96940334	T-47D	breast:	n/a
22	chr2:96940284-96940334	HEK293	kidney:	embryo
23	chr2:96944236-96944286	AG04449	skin:	fetal
24	chr2:96940284-96940334	NT2-D1	testis:	n/a
25	chr2:96940284-96940334	HIPEpiC	eye:	n/a
26	chr2:96944236-96944286	GM12892	blood:	n/a
27	chr2:96944360-96944410	AG04449	skin:	fetal
28	chr2:96944360-96944410	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:96944360-96944410	NHBE	bronchial:	n/a
30	chr2:96937097-96937147	HCM	heart:	n/a
31	chr2:96937097-96937147	ProgFib	skin:	n/a
32	chr2:96937097-96937147	SK-N-MC	brain:	n/a
33	chr2:96944236-96944286	ovcar-3	ovarian:	n/a
34	chr2:96944236-96944286	Caco-2	colon:	n/a
35	chr2:96940284-96940334	HepG2	liver:	n/a
36	chr2:96940284-96940334	H1-hESC	embryonic stem cell:	embryo
37	chr2:96944360-96944410	SK-N-MC	brain:	n/a
38	chr2:96944360-96944410	HL-60	blood:	n/a
39	chr2:96944236-96944286	SAEC	small airway:	n/a
40	chr2:96944360-96944410	Hepatocyte	liver:	n/a
41	chr2:96940284-96940334	HCF	heart:	n/a
42	chr2:96937097-96937147	HCPEpiC	choroid plexus:	n/a
43	chr2:96937097-96937147	GM12892	blood:	n/a
44	chr2:96944236-96944286	HCPEpiC	choroid plexus:	n/a
45	chr2:96944236-96944286	SK-N-MC	brain:	n/a
46	chr2:96944236-96944286	AG09319	gingival:	n/a
47	chr2:96940284-96940334	GM12878	blood:	n/a
48	chr2:96944360-96944410	BJ	skin:	n/a
49	chr2:96940284-96940334	SKMC	muscle:	n/a
50	chr2:96944360-96944410	HRE	kidney:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:96950941..96952734-chr2:96952916..96955676,2	K562	blood:
2	chr2:96936840..96938962-chr2:96985543..96987656,2	MCF-7	breast:
3	chr2:96930148..96938607-chr2:96966008..96973188,21	MCF-7	breast:
4	chr2:96938019..96939649-chr2:96946128..96948326,2	MCF-7	breast:
5	chr2:96948398..96950278-chr2:96962881..96965355,2	MCF-7	breast:
6	chr2:96929774..96935946-chr2:96940519..96946631,7	K562	blood:
7	chr2:96946329..96948164-chr2:96950653..96953399,2	K562	blood:
8	chr2:96934617..96938002-chr2:96987663..96991573,3	K562	blood:
9	chr2:96939630..96942244-chr2:96954268..96957042,3	K562	blood:
10	chr2:96942551..96945806-chr2:96946996..96949678,4	K562	blood:
11	chr2:96939921..96941741-chr2:96942153..96943823,2	MCF-7	breast:
12	chr2:96935272..96937348-chr2:96947447..96949383,2	K562	blood:
13	chr2:96940057..96942463-chr2:96949607..96951912,2	MCF-7	breast:
14	chr2:96930149..96935122-chr2:96939914..96944095,6	MCF-7	breast:
15	chr2:96864705..96867653-chr2:96939158..96942090,2	MCF-7	breast:
16	chr2:96934609..96937384-chr2:96952296..96954901,2	MCF-7	breast:
17	chr2:96946287..96947910-chr2:96970325..96972157,2	MCF-7	breast:
18	chr2:96939108..96946297-chr2:96949498..96959663,15	MCF-7	breast:
19	chr2:96939108..96946297-chr2:96949498..96959663,15	MCF-7	breast:
20	chr2:96946329..96948164-chr2:96950653..96953399,2	K562	blood:
21	chr2:96937785..96940633-chr2:96966720..96968269,2	K562	blood:
22	chr2:96936395..96940280-chr2:96940621..96945633,7	K562	blood:
23	chr2:96942551..96945806-chr2:96946996..96949678,4	K562	blood:
24	chr2:96935786..96937903-chr2:96948870..96951408,2	MCF-7	breast:
25	chr2:96940315..96942248-chr2:96957003..96958754,2	MCF-7	breast:
26	chr2:96939921..96941741-chr2:96942153..96943823,2	MCF-7	breast:
27	chr2:96935062..96937810-chr2:97000654..97003812,3	MCF-7	breast:
28	chr2:96936670..96937551-chr7:30633906..30634472,2	NB4	blood:
29	chr2:96941125..96943370-chr2:96972215..96974002,2	K562	blood:
30	chr2:96934413..96937230-chr2:96969465..96972171,2	MCF-7	breast:

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SNRNP200	hsa-miR-425-5p	chr2:96950895-96950911
2	SNRNP200	hsa-miR-425-5p	chr2:96940560-96940582
3	SNRNP200	hsa-miR-149-5p	chr2:96947314-96947337
4	CIAO1	hsa-let-7b-5p	chr2:96937090-96937098
5	CIAO1	hsa-miR-193b-3p	chr2:96939018-96939039

Variant related genes	Relation type
SNRNP200	TF binding region
TMEM127	TF binding region
SNRNP200	CpG island
TMEM127	CpG island
ENSG00000121152	chromatin interactions
ENSG00000135956	chromatin interactions
ENSG00000230747	chromatin interactions
ENSG00000198885	chromatin interactions
ENSG00000106105	chromatin interactions
ENSG00000144028	chromatin interactions
ENSG00000196295	chromatin interactions
ENSG00000144021	chromatin interactions

Extended variants
information (count: 600 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563004583	chr2:96936293-96936294	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs182895469	chr2:96936341-96936342	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs139159436	chr2:96936404-96936405	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs141745947	chr2:96936417-96936418	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs527996195	chr2:96936442-96936443	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs547649023	chr2:96936501-96936502	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs150549574	chr2:96936520-96936521	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs185308307	chr2:96936526-96936527	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs531540380	chr2:96936548-96936549	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs558221767	chr2:96936560-96936561	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs139626749	chr2:96936606-96936607	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs539708766	chr2:96936622-96936623	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs537398491	chr2:96936648-96936649	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs554560551	chr2:96936669-96936670	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs552135803	chr2:96936780-96936781	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs574608845	chr2:96936794-96936795	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs201603533	chr2:96936810-96936811	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs372825821	chr2:96936821-96936822	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs200681392	chr2:96936838-96936839	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs530598937	chr2:96936861-96936862	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs374736407	chr2:96936865-96936866	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs367694646	chr2:96936892-96936893	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs199705771	chr2:96936894-96936895	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs371499283	chr2:96936901-96936902	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs201628543	chr2:96936924-96936925	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs112998874	chr2:96936936-96936937	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs150585467	chr2:96936960-96936961	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs374921480	chr2:96936968-96936969	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs191488251	chr2:96936989-96936990	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs369287426	chr2:96937011-96937012	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs34335242	chr2:96937030-96937031	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs149718420	chr2:96937065-96937066	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs139155173	chr2:96937072-96937073	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs199858380	chr2:96937073-96937074	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs570240999	chr2:96937074-96937075	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs3087589	chr2:96937086-96937087	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs369770870	chr2:96937094-96937095	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region miRNA target site	7 gene(s)	Overlapped CNVs	n/a
38	rs373876864	chr2:96937098-96937099	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region miRNA target site	7 gene(s)	Overlapped CNVs	n/a
39	rs377064367	chr2:96937114-96937115	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs562137591	chr2:96937126-96937127	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs371515038	chr2:96937129-96937130	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs369074719	chr2:96937130-96937131	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs372688622	chr2:96937131-96937132	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs74604002	chr2:96937152-96937153	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs554843660	chr2:96937154-96937155	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs1044594	chr2:96937296-96937297	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs533346816	chr2:96937340-96937341	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs144205476	chr2:96937343-96937344	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs549966222	chr2:96937385-96937386	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs116173122	chr2:96937444-96937445	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21990379	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96932600-96941600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:96932800-96970400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:96933200-96938200	Strong transcription	H9 Cell Line	embryonic stem cell
4	chr2:96933200-96970200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:96933200-96970400	Weak transcription	Right Atrium	heart
6	chr2:96933400-96938000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:96933400-96938200	Strong transcription	H1 Cell Line	embryonic stem cell
8	chr2:96933400-96941000	Strong transcription	NHEK	skin
9	chr2:96933400-96956800	Strong transcription	Placenta	Placenta
10	chr2:96933400-96957400	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr2:96933400-96968800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:96933400-96969000	Strong transcription	Left Ventricle	heart
13	chr2:96933400-96969200	Strong transcription	Rectal Mucosa Donor 31	rectum
14	chr2:96933400-96969400	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr2:96933400-96969400	Strong transcription	Brain Inferior Temporal Lobe	brain
16	chr2:96933400-96970200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:96933400-96970200	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr2:96933400-96970200	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr2:96933400-96970200	Strong transcription	Fetal Lung	lung
20	chr2:96933400-96970200	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr2:96933600-96936800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr2:96933600-96936800	Weak transcription	Psoas Muscle	Psoas
23	chr2:96933600-96937200	Strong transcription	Right Ventricle	heart
24	chr2:96933600-96938000	Strong transcription	Brain Substantia Nigra	brain
25	chr2:96933600-96938400	Strong transcription	HSMMtube	muscle
26	chr2:96933600-96938800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:96933600-96938800	Strong transcription	Colon Smooth Muscle	Colon
28	chr2:96933600-96939600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr2:96933600-96943000	Weak transcription	Fetal Heart	heart
30	chr2:96933600-96960200	Strong transcription	Liver	Liver
31	chr2:96933600-96965800	Strong transcription	Lung	lung
32	chr2:96933600-96966800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr2:96933600-96966800	Strong transcription	Brain Germinal Matrix	brain
34	chr2:96933600-96967200	Strong transcription	Brain Angular Gyrus	brain
35	chr2:96933600-96969400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr2:96933600-96969400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr2:96933600-96969400	Strong transcription	Fetal Muscle Trunk	muscle
38	chr2:96933600-96969600	Strong transcription	Duodenum Mucosa	Duodenum
39	chr2:96933600-96969600	Strong transcription	Stomach Smooth Muscle	stomach
40	chr2:96933600-96969800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:96933600-96969800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:96933600-96969800	Strong transcription	Fetal Intestine Small	intestine
43	chr2:96933600-96969800	Strong transcription	Fetal Stomach	stomach
44	chr2:96933600-96969800	Strong transcription	Hela-S3	cervix
45	chr2:96933600-96970000	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr2:96933600-96970000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
47	chr2:96933600-96970000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr2:96933600-96970200	Strong transcription	Primary B cells from peripheral blood	blood
49	chr2:96933600-96970200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr2:96933600-96970200	Strong transcription	Fetal Muscle Leg	muscle

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