Variant report

Variant	nsv875749
Chromosome Location	chr2:209022909-209062388
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:514)
CpG islands
(count:793)
Chromatin interactive
region (count:27)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:209040108-209040387	K562	blood:	n/a	n/a
2	ARID3A	chr2:209040041-209040430	HepG2	liver:	n/a	n/a
3	ATF1	chr2:209036916-209037257	K562	blood:	n/a	n/a
4	BACH1	chr2:209036897-209037049	K562	blood:	n/a	n/a
5	BCLAF1	chr2:209040035-209040305	GM12878	blood:	n/a	n/a
6	BCLAF1	chr2:209040059-209040456	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:209036792-209037173	HepG2	liver:	n/a	chr2:209036955-209036964 chr2:209036950-209036971
8	BHLHE40	chr2:209040130-209040348	K562	blood:	n/a	n/a
9	BHLHE40	chr2:209039203-209039447	K562	blood:	n/a	n/a
10	BHLHE40	chr2:209036991-209037029	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:209036726-209037189	K562	blood:	n/a	chr2:209036955-209036964 chr2:209036950-209036971
12	CBX3	chr2:209036804-209037150	K562	blood:	n/a	n/a
13	CBX3	chr2:209039958-209040402	K562	blood:	n/a	n/a
14	CEBPB	chr2:209037651-209037883	A549	lung:	n/a	chr2:209037793-209037804
15	CEBPB	chr2:209037731-209037841	H1-hESC	embryonic stem cell:	n/a	chr2:209037793-209037804
16	CEBPB	chr2:209039968-209040482	K562	blood:	n/a	n/a
17	CEBPB	chr2:209040087-209040406	A549	lung:	n/a	n/a
18	CEBPB	chr2:209037544-209037877	IMR90	lung:	n/a	chr2:209037793-209037804
19	CEBPB	chr2:209037671-209037918	K562	blood:	n/a	chr2:209037793-209037804
20	CEBPB	chr2:209043905-209044275	HepG2	liver:	n/a	chr2:209044080-209044091
21	CEBPB	chr2:209037644-209037894	K562	blood:	n/a	chr2:209037793-209037804
22	CEBPB	chr2:209039995-209040438	MCF-7	breast:	n/a	n/a
23	CEBPB	chr2:209043880-209044312	MCF-7	breast:	n/a	chr2:209044080-209044091
24	CEBPB	chr2:209043897-209044285	HepG2	liver:	n/a	chr2:209044080-209044091
25	CEBPB	chr2:209043891-209044214	K562	blood:	n/a	chr2:209044080-209044091
26	CEBPB	chr2:209040062-209040418	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:209040135-209040344	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:209043922-209044294	HepG2	liver:	n/a	chr2:209044080-209044091
29	CEBPB	chr2:209040104-209040463	A549	lung:	n/a	n/a
30	CEBPB	chr2:209043915-209044258	K562	blood:	n/a	chr2:209044080-209044091
31	CEBPB	chr2:209048700-209048981	H1-hESC	embryonic stem cell:	n/a	chr2:209048819-209048830
32	CEBPB	chr2:209040042-209040396	K562	blood:	n/a	n/a
33	CEBPB	chr2:209040071-209040454	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:209040079-209040454	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:209043994-209044214	HepG2	liver:	n/a	chr2:209044080-209044091
36	CEBPB	chr2:209048718-209048898	HepG2	liver:	n/a	chr2:209048819-209048830
37	CEBPB	chr2:209040049-209040477	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr2:209040025-209040475	MCF-7	breast:	n/a	n/a
39	CEBPB	chr2:209040017-209040455	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr2:209040063-209040484	A549	lung:	n/a	n/a
41	CEBPB	chr2:209028041-209028161	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:209043908-209044263	H1-hESC	embryonic stem cell:	n/a	chr2:209044080-209044091
43	CEBPB	chr2:209048683-209048969	HepG2	liver:	n/a	chr2:209048819-209048830
44	CEBPB	chr2:209037690-209037847	HepG2	liver:	n/a	chr2:209037793-209037804
45	CEBPB	chr2:209039992-209040447	HepG2	liver:	n/a	n/a
46	CEBPD	chr2:209043968-209044174	HepG2	liver:	n/a	n/a
47	CEBPD	chr2:209043978-209044221	HepG2	liver:	n/a	n/a
48	CHD2	chr2:209044056-209044267	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr2:209040098-209040315	A549	lung:	n/a	n/a
50	CTBP2	chr2:209048380-209049301	H1-hESC	embryonic stem cell:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209029782-209029832	PFSK-1	brain:	n/a
2	chr2:209054670-209054720	PANC-1	pancreas:	n/a
3	chr2:209028059-209028109	Hela-S3	cervix:	n/a
4	chr2:209028059-209028109	CMK	blood:	n/a
5	chr2:209029594-209029644	NHDF-neo	bronchial:	n/a
6	chr2:209055251-209055301	T-47D	breast:	n/a
7	chr2:209025539-209025589	HNPCEpiC	eye:	n/a
8	chr2:209028478-209028528	HRE	kidney:	n/a
9	chr2:209028399-209028449	BJ	skin:	n/a
10	chr2:209055151-209055201	MCF10A-Er-Src	breast:	n/a
11	chr2:209054740-209054790	AG09319	gingival:	n/a
12	chr2:209055251-209055301	PrEC	prostate:	n/a
13	chr2:209040082-209040132	ovcar-3	ovarian:	n/a
14	chr2:209054670-209054720	ovcar-3	ovarian:	n/a
15	chr2:209040082-209040132	NHDF-neo	bronchial:	n/a
16	chr2:209028399-209028449	AG04450	lung:	fetal
17	chr2:209028478-209028528	SK-N-SH_RA	brain:	n/a
18	chr2:209054740-209054790	A549	lung:	n/a
19	chr2:209025539-209025589	NB4	blood:	n/a
20	chr2:209029690-209029740	HEEpiC	esophagus:	n/a
21	chr2:209028478-209028528	AG09319	gingival:	n/a
22	chr2:209028059-209028109	ovcar-3	ovarian:	n/a
23	chr2:209025539-209025589	HRE	kidney:	n/a
24	chr2:209054670-209054720	SK-N-MC	brain:	n/a
25	chr2:209029690-209029740	HAEpiC	amniotic membrane:	n/a
26	chr2:209040082-209040132	GM06990	blood:	n/a
27	chr2:209055251-209055301	HUVEC	blood vessel:	n/a
28	chr2:209055151-209055201	Hepatocyte	liver:	n/a
29	chr2:209029782-209029832	H1-hESC	embryonic stem cell:	embryo
30	chr2:209028059-209028109	ProgFib	skin:	n/a
31	chr2:209028059-209028109	NHBE	bronchial:	n/a
32	chr2:209028399-209028449	Hela-S3	cervix:	n/a
33	chr2:209040082-209040132	NB4	blood:	n/a
34	chr2:209029690-209029740	K562	blood:	n/a
35	chr2:209054740-209054790	AG10803	skin:	n/a
36	chr2:209029594-209029644	LNCaP	prostate:	n/a
37	chr2:209054670-209054720	RPTEC	kidney:	n/a
38	chr2:209029782-209029832	CMK	blood:	n/a
39	chr2:209029594-209029644	HIPEpiC	eye:	n/a
40	chr2:209048830-209048880	NB4	blood:	n/a
41	chr2:209028399-209028449	H1-hESC	embryonic stem cell:	embryo
42	chr2:209029690-209029740	HCPEpiC	choroid plexus:	n/a
43	chr2:209029594-209029644	Hepatocyte	liver:	n/a
44	chr2:209048830-209048880	LNCaP	prostate:	n/a
45	chr2:209048830-209048880	SK-N-MC	brain:	n/a
46	chr2:209028399-209028449	HEEpiC	esophagus:	n/a
47	chr2:209048830-209048880	HCT-116	colon:	n/a
48	chr2:209054670-209054720	A549	lung:	n/a
49	chr2:209040082-209040132	NT2-D1	testis:	n/a
50	chr2:209054740-209054790	K562	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:19991747..19994521-chr2:209032147..209035018,4	K562	blood:
2	chr2:209040088..209040688-chr2:209118748..209120316,4	K562	blood:
3	chr2:209058168..209060792-chr2:209061919..209063895,2	K562	blood:
4	chr2:209033532..209035428-chr2:209036949..209038570,2	MCF-7	breast:
5	chr2:209039807..209040681-chr2:209119247..209120525,5	MCF-7	breast:
6	chr2:209060491..209062065-chr2:209066501..209069096,2	K562	blood:
7	chr2:209040053..209040651-chr2:209133538..209134369,3	K562	blood:
8	chr2:209059939..209061469-chr2:209069888..209071988,2	K562	blood:
9	chr17:19995540..19998202-chr2:209032220..209035134,2	MCF-7	breast:
10	chr2:209049851..209051700-chr2:209064881..209067497,2	K562	blood:
11	chr2:209050833..209051384-chr5:23573266..23573766,2	MCF-7	breast:
12	chr2:209058168..209060792-chr2:209061919..209063895,2	K562	blood:
13	chr2:209033805..209035560-chr2:209037521..209040634,3	K562	blood:
14	chr2:209043347..209044006-chr2:209118780..209119320,2	MCF-7	breast:
15	chr2:209034002..209036462-chr2:209130730..209132491,2	K562	blood:
16	chr2:209033532..209035428-chr2:209036949..209038570,2	MCF-7	breast:
17	chr2:209039733..209040833-chr2:209118699..209120498,12	MCF-7	breast:
18	chr2:209027080..209028800-chr2:209034737..209037524,2	K562	blood:
19	chr2:209033805..209035560-chr2:209037521..209040634,3	K562	blood:
20	chr2:209041162..209042836-chr2:209051785..209054428,2	K562	blood:
21	chr2:209041162..209042836-chr2:209051785..209054428,2	K562	blood:
22	chr2:209039776..209040279-chr2:209119196..209119817,2	MCF-7	breast:
23	chr2:209028147..209030842-chr2:209033531..209035644,2	MCF-7	breast:
24	chr2:209058318..209061036-chr2:209107934..209110316,2	MCF-7	breast:
25	chr17:19991773..19994998-chr2:209032034..209035004,3	K562	blood:
26	chr2:209048413..209050423-chr2:209125192..209127904,2	K562	blood:
27	chr2:209045281..209046929-chr2:209048317..209050730,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIKFYVE-4	chr2:209048753-209048776	NONHSAT076630

No data

Variant related genes	Relation type
CRYGA	TF binding region
C2orf80	TF binding region
CRYGA	CpG island
C2orf80	CpG island
ENSG00000231908	chromatin interactions
ENSG00000168582	chromatin interactions
ENSG00000115020	chromatin interactions
ENSG00000188674	chromatin interactions
ENSG00000138413	chromatin interactions

Extended variants
information (count: 1580 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1580 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375136997	chr2:209026817-209026818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs369507981	chr2:209026819-209026820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190623391	chr2:209026841-209026842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575021924	chr2:209026862-209026863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534633358	chr2:209026863-209026864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369627570	chr2:209026932-209026933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113422245	chr2:209026940-209026941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560356502	chr2:209026960-209026961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs62194805	chr2:209027278-209027279	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs187640046	chr2:209027304-209027305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558884588	chr2:209027307-209027308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199579622	chr2:209027346-209027347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148014189	chr2:209027347-209027348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs66517860	chr2:209027348-209027349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs71036984	chr2:209027352-209027353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147239549	chr2:209027353-209027354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs796278	chr2:209027424-209027425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs538523056	chr2:209027468-209027469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190811055	chr2:209027477-209027478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574908412	chr2:209027478-209027479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534137552	chr2:209027480-209027481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554247968	chr2:209027490-209027491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577255605	chr2:209027506-209027507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138647173	chr2:209027550-209027551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200926418	chr2:209027569-209027570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77258912	chr2:209027571-209027572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545233683	chr2:209027581-209027582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564906411	chr2:209027603-209027604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs13389724	chr2:209027608-209027609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78120045	chr2:209027609-209027610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575189502	chr2:209027613-209027614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78881381	chr2:209027626-209027627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554963992	chr2:209027627-209027628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544115247	chr2:209027630-209027631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560820763	chr2:209027640-209027641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10932243	chr2:209027654-209027655	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs546270681	chr2:209027665-209027666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183421693	chr2:209027670-209027671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532087964	chr2:209027749-209027750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35825947	chr2:209027773-209027774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572790842	chr2:209027776-209027777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541244627	chr2:209027777-209027778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552771632	chr2:209027786-209027787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73986526	chr2:209027808-209027809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs796279	chr2:209027871-209027872	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs370025596	chr2:209027889-209027890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77906750	chr2:209027912-209027913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188362743	chr2:209027929-209027930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370522253	chr2:209027932-209027933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139353014	chr2:209027941-209027942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209026800-209027000	Enhancers	Fetal Brain Female	brain
2	chr2:209027200-209028200	Weak transcription	Fetal Brain Female	brain
3	chr2:209028000-209028200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:209028000-209028400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:209028000-209028600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr2:209028000-209028600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:209028000-209028800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:209028200-209028600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr2:209028200-209028600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr2:209028200-209029600	Enhancers	H9 Cell Line	embryonic stem cell
11	chr2:209028200-209030400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:209028200-209030600	Enhancers	Fetal Brain Female	brain
13	chr2:209028200-209031800	Enhancers	Fetal Brain Male	brain
14	chr2:209028200-209033200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr2:209028600-209028800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:209028600-209029000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:209028600-209031600	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr2:209028600-209033400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr2:209028600-209040400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:209028800-209034800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:209029000-209029400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:209029400-209029600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:209029400-209029600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr2:209029800-209040000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr2:209030600-209040400	Weak transcription	Fetal Brain Female	brain
26	chr2:209031600-209039400	Strong transcription	Cortex derived primary cultured neurospheres	brain
27	chr2:209031800-209039800	Weak transcription	Fetal Brain Male	brain
28	chr2:209032400-209032800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr2:209032800-209040600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr2:209033200-209037600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:209033400-209033600	Enhancers	K562	blood
32	chr2:209033400-209033800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr2:209033600-209036400	Weak transcription	K562	blood
34	chr2:209033600-209040000	Weak transcription	Brain Germinal Matrix	brain
35	chr2:209034600-209035000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr2:209034800-209035200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:209035200-209040400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:209036400-209036600	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr2:209036400-209036800	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr2:209036400-209037400	Enhancers	Primary hematopoietic stem cells	blood
41	chr2:209036400-209037800	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr2:209036400-209037800	Enhancers	K562	blood
43	chr2:209036400-209038600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr2:209036600-209037600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:209036600-209037800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr2:209036600-209038000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr2:209036600-209040200	Weak transcription	Brain Cingulate Gyrus	brain
48	chr2:209036800-209037000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr2:209036800-209037200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
50	chr2:209036800-209037400	Bivalent Enhancer	HepG2	liver

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