Variant report

Variant	nsv469161
Chromosome Location	chr12:21507702-21555691
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:185)
CpG islands
(count:428)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:185 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:21510090-21510388	K562	blood:	n/a	n/a
2	BCL3	chr12:21507707-21507938	GM12878	blood:	n/a	chr12:21507798-21507807 chr12:21507799-21507808
3	CEBPB	chr12:21530522-21530768	HepG2	liver:	n/a	chr12:21530683-21530696
4	CEBPB	chr12:21532177-21532548	H1-hESC	embryonic stem cell:	n/a	chr12:21532354-21532365
5	CEBPB	chr12:21532151-21532558	K562	blood:	n/a	chr12:21532354-21532365
6	CEBPB	chr12:21532175-21532550	IMR90	lung:	n/a	chr12:21532354-21532365
7	CEBPB	chr12:21532153-21532556	A549	lung:	n/a	chr12:21532354-21532365
8	CEBPB	chr12:21532171-21532556	A549	lung:	n/a	chr12:21532354-21532365
9	CEBPB	chr12:21532161-21532522	K562	blood:	n/a	chr12:21532354-21532365
10	CEBPB	chr12:21511288-21511491	HepG2	liver:	n/a	chr12:21511352-21511369
11	CEBPB	chr12:21546630-21546943	IMR90	lung:	n/a	chr12:21546784-21546795
12	CEBPB	chr12:21532051-21532632	A549	lung:	n/a	chr12:21532354-21532365
13	CEBPB	chr12:21532170-21532544	HepG2	liver:	n/a	chr12:21532354-21532365
14	CEBPB	chr12:21547658-21547858	K562	blood:	n/a	chr12:21547721-21547734
15	CEBPB	chr12:21532183-21532548	Hela-S3	cervix:	n/a	chr12:21532354-21532365
16	CEBPB	chr12:21532225-21532408	K562	blood:	n/a	chr12:21532354-21532365
17	CEBPB	chr12:21532134-21532564	ECC-1	luminal epithelium:	n/a	chr12:21532354-21532365
18	CEBPB	chr12:21511236-21511525	K562	blood:	n/a	chr12:21511352-21511369
19	CEBPB	chr12:21546696-21546939	A549	lung:	n/a	chr12:21546784-21546795
20	CEBPB	chr12:21532119-21532562	ECC-1	luminal epithelium:	n/a	chr12:21532354-21532365
21	CEBPB	chr12:21548420-21548434	K562	blood:	n/a	n/a
22	CEBPB	chr12:21546640-21546957	HepG2	liver:	n/a	chr12:21546784-21546795
23	CEBPB	chr12:21546588-21546963	K562	blood:	n/a	chr12:21546784-21546795
24	CTCF	chr12:21524128-21524168	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr12:21524143-21524211	GM10248	blood:	n/a	n/a
26	CTCF	chr12:21524060-21524210	Caco-2	colon:	n/a	n/a
27	CTCF	chr12:21510388-21510533	K562	blood:	n/a	n/a
28	CTCF	chr12:21524160-21524310	NB4	blood:	n/a	n/a
29	CTCF	chr12:21524060-21524210	HMF	breast:	n/a	n/a
30	CTCF	chr12:21524100-21524250	HEK293	kidney:	n/a	n/a
31	CTCF	chr12:21524100-21524250	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr12:21524080-21524230	HFF	foreskin:	n/a	n/a
33	CTCF	chr12:21524060-21524293	K562	blood:	n/a	n/a
34	CTCF	chr12:21524222-21524236	LNCaP	prostate:	n/a	n/a
35	CTCF	chr12:21524111-21524227	GM12892	blood:	n/a	n/a
36	CTCF	chr12:21524829-21524869	A549	lung:	n/a	n/a
37	CTCF	chr12:21524100-21524250	GM12871	blood:	n/a	n/a
38	CTCF	chr12:21524080-21524230	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr12:21524085-21524211	HepG2	liver:	n/a	n/a
40	CTCF	chr12:21524626-21524710	GM10248	blood:	n/a	n/a
41	CTCF	chr12:21523980-21524130	GM12872	blood:	n/a	n/a
42	CTCF	chr12:21524117-21524206	A549	lung:	n/a	n/a
43	CTCF	chr12:21524080-21524230	GM12874	blood:	n/a	n/a
44	CTCF	chr12:21540600-21540750	GM12864	blood:	n/a	n/a
45	CTCF	chr12:21524128-21524198	Medullo	brain:	n/a	n/a
46	CTCF	chr12:21520371-21520400	LNCaP	prostate:	n/a	n/a
47	CTCF	chr12:21524107-21524292	GM12878	blood:	n/a	n/a
48	CTCF	chr12:21524080-21524230	BE2_C	brain:	n/a	n/a
49	CTCF	chr12:21524111-21524194	ProgFib	skin:	n/a	n/a
50	CTCF	chr12:21524135-21524191	GM19240	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21531643-21531693	HRPEpiC	eye:	n/a
2	chr12:21531643-21531693	HRPEpiC	eye:	n/a
3	chr12:21525662-21525712	HepG2	liver:	n/a
4	chr12:21524305-21524355	PrEC	prostate:	n/a
5	chr12:21524305-21524355	ProgFib	skin:	n/a
6	chr12:21509398-21509448	U87	brain:	n/a
7	chr12:21524305-21524355	Hepatocyte	liver:	n/a
8	chr12:21524305-21524355	HUVEC	blood vessel:	n/a
9	chr12:21525662-21525712	HMEC	breast:	n/a
10	chr12:21531187-21531237	HRPEpiC	eye:	n/a
11	chr12:21548228-21548278	NT2-D1	testis:	n/a
12	chr12:21531643-21531693	NH-A	brain:	n/a
13	chr12:21509398-21509448	GM12891	blood:	n/a
14	chr12:21548228-21548278	A549	lung:	n/a
15	chr12:21524305-21524355	AG04450	lung:	fetal
16	chr12:21524305-21524355	Jurkat	blood:	n/a
17	chr12:21531643-21531693	HCT-116	colon:	n/a
18	chr12:21531187-21531237	SK-N-MC	brain:	n/a
19	chr12:21547892-21547942	HEK293	kidney:	embryo
20	chr12:21547892-21547942	SK-N-SH	brain:	n/a
21	chr12:21524305-21524355	HRCEpiC	kidney:	n/a
22	chr12:21547892-21547942	Hela-S3	cervix:	n/a
23	chr12:21531643-21531693	HPAEpiC	pulmonary alveolar:	n/a
24	chr12:21531187-21531237	HCT-116	colon:	n/a
25	chr12:21509398-21509448	AoSMC	blood vessel:	n/a
26	chr12:21531643-21531693	HMEC	breast:	n/a
27	chr12:21547892-21547942	AG09319	gingival:	n/a
28	chr12:21509398-21509448	ProgFib	skin:	n/a
29	chr12:21548228-21548278	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:21525662-21525712	AG09319	gingival:	n/a
31	chr12:21547892-21547942	HPAEpiC	pulmonary alveolar:	n/a
32	chr12:21524305-21524355	AG09319	gingival:	n/a
33	chr12:21524305-21524355	CMK	blood:	n/a
34	chr12:21531643-21531693	A549	lung:	n/a
35	chr12:21524305-21524355	HEK293	kidney:	embryo
36	chr12:21547892-21547942	AG04449	skin:	fetal
37	chr12:21547892-21547942	NHDF-neo	bronchial:	n/a
38	chr12:21509398-21509448	Hela-S3	cervix:	n/a
39	chr12:21531187-21531237	AG09309	skin:	n/a
40	chr12:21524305-21524355	Caco-2	colon:	n/a
41	chr12:21524305-21524355	ovcar-3	ovarian:	n/a
42	chr12:21531187-21531237	AG04449	skin:	fetal
43	chr12:21548228-21548278	NB4	blood:	n/a
44	chr12:21547892-21547942	Caco-2	colon:	n/a
45	chr12:21531643-21531693	T-47D	breast:	n/a
46	chr12:21547892-21547942	AG09309	skin:	n/a
47	chr12:21548228-21548278	Hepatocyte	liver:	n/a
48	chr12:21525662-21525712	PANC-1	pancreas:	n/a
49	chr12:21525662-21525712	ECC-1	luminal epithelium:	n/a
50	chr12:21531187-21531237	PFSK-1	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:21507792..21510095-chr12:21510870..21513071,2	K562	blood:
2	chr12:21526840..21530031-chr12:21536800..21540438,4	K562	blood:
3	chr12:21526840..21530031-chr12:21536800..21540438,4	K562	blood:
4	chr12:21526910..21529766-chr12:21530369..21533433,3	K562	blood:
5	chr12:21544378..21545319-chr4:2144383..2145235,2	MCF-7	breast:
6	chr12:21509512..21511377-chr12:21523950..21526007,2	K562	blood:
7	chr12:21528193..21534017-chr12:21534075..21538760,6	K562	blood:
8	chr12:21527361..21529300-chr12:21544200..21546826,2	K562	blood:
9	chr12:21502651..21506189-chr12:21507967..21511740,6	K562	blood:
10	chr12:21528193..21534017-chr12:21534075..21538760,6	K562	blood:
11	chr12:21527361..21529300-chr12:21544200..21546826,2	K562	blood:
12	chr12:21526910..21529766-chr12:21530369..21533433,3	K562	blood:

No data

Variant related genes	Relation type
IAPP	TF binding region
SLCO1A2	TF binding region
IAPP	CpG island
SLCO1A2	CpG island
ENSG00000121351	chromatin interactions

Extended variants
information (count: 1284 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11045994	chr12:21507702-21507703	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572182218	chr12:21507703-21507704	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs541220935	chr12:21507715-21507716	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs368176494	chr12:21507729-21507730	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs564323235	chr12:21507776-21507777	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs187117164	chr12:21507864-21507865	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs150793691	chr12:21507884-21507885	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs563449769	chr12:21507940-21507941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532580557	chr12:21507970-21507971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191597781	chr12:21507971-21507972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114834117	chr12:21507993-21507994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs117624721	chr12:21507998-21507999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183701217	chr12:21508027-21508028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528812972	chr12:21508088-21508089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs75756847	chr12:21508114-21508115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551243198	chr12:21508156-21508157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs11045995	chr12:21508178-21508179	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs530709501	chr12:21508215-21508216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139221479	chr12:21508225-21508226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs10841797	chr12:21508230-21508231	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs190523302	chr12:21508327-21508328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149770486	chr12:21508333-21508334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555107022	chr12:21508354-21508355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572165663	chr12:21508406-21508407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541159463	chr12:21508423-21508424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs367667567	chr12:21508442-21508443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371459243	chr12:21508457-21508458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577880197	chr12:21508478-21508479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543276289	chr12:21508491-21508492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563553272	chr12:21508499-21508500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528437731	chr12:21508503-21508504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529184876	chr12:21508525-21508526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12820524	chr12:21508557-21508558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs193267690	chr12:21508574-21508575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11834777	chr12:21508578-21508579	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs185440200	chr12:21508716-21508717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534127848	chr12:21508759-21508760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374439292	chr12:21508762-21508763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11834836	chr12:21508881-21508882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs368663699	chr12:21508939-21508940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547116593	chr12:21509080-21509081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190280667	chr12:21509152-21509153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547084887	chr12:21509173-21509174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550114588	chr12:21509200-21509201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141604639	chr12:21509267-21509268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535816377	chr12:21509273-21509274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34744403	chr12:21509289-21509290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs117918930	chr12:21509323-21509324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376550525	chr12:21509359-21509360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570196252	chr12:21509398-21509399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21504200-21513200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:21506200-21508600	Enhancers	K562	blood
3	chr12:21506600-21509400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr12:21506600-21509400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr12:21507200-21507800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr12:21507400-21508000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr12:21507800-21508400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr12:21508400-21509800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr12:21508600-21510000	Weak transcription	K562	blood
10	chr12:21509400-21509600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr12:21509400-21509800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr12:21509600-21510000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr12:21510000-21510200	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr12:21510000-21510200	Flanking Active TSS	K562	blood
15	chr12:21510000-21510600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr12:21510200-21510400	Enhancers	K562	blood
17	chr12:21510400-21510600	Flanking Active TSS	K562	blood
18	chr12:21510600-21511000	Enhancers	K562	blood
19	chr12:21512400-21513000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr12:21513000-21513200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
21	chr12:21513000-21513400	Enhancers	Hela-S3	cervix
22	chr12:21513400-21513800	Active TSS	Hela-S3	cervix
23	chr12:21519800-21520200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr12:21519800-21521200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr12:21520000-21521200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr12:21520200-21520600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr12:21520200-21520600	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr12:21520400-21520800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr12:21520600-21529200	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr12:21521000-21521400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr12:21521200-21526400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr12:21522000-21523400	Enhancers	HUVEC	blood vessel
33	chr12:21522200-21522800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr12:21522200-21522800	Enhancers	Muscle Satellite Cultured Cells	--
35	chr12:21522200-21523000	Enhancers	Osteobl	bone
36	chr12:21522600-21522800	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr12:21523400-21523800	Weak transcription	HUVEC	blood vessel
38	chr12:21523800-21524200	Enhancers	HUVEC	blood vessel
39	chr12:21524000-21524200	Weak transcription	K562	blood
40	chr12:21524200-21524400	Enhancers	K562	blood
41	chr12:21524400-21525200	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr12:21525200-21525400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr12:21525400-21531400	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr12:21526400-21527400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr12:21526800-21527400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr12:21527400-21532200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr12:21528800-21529400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr12:21529200-21529400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr12:21531400-21532200	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr12:21532000-21532800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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