Variant report

Variant	nsv1051648
Chromosome Location	chr12:31069125-31103671
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	CEBPB	chr12:31085152-31085428	A549	lung:	n/a	chr12:31085248-31085259
2	CEBPB	chr12:31079297-31079429	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr12:31085140-31085384	K562	blood:	n/a	chr12:31085248-31085259
4	CEBPB	chr12:31092097-31092209	HepG2	liver:	n/a	chr12:31092125-31092136
5	CEBPB	chr12:31085137-31085429	IMR90	lung:	n/a	chr12:31085248-31085259
6	CEBPB	chr12:31085137-31085427	HepG2	liver:	n/a	chr12:31085248-31085259
7	CHD1	chr12:31079467-31079488	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr12:31078905-31079452	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTBP2	chr12:31078500-31079604	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr12:31099700-31099850	SK-N-SH_RA	brain:	n/a	chr12:31099817-31099826
11	CTCF	chr12:31089095-31089260	MCF-7	breast:	n/a	n/a
12	CTCF	chr12:31079420-31079570	HCM	heart:	n/a	chr12:31079543-31079551
13	CTCF	chr12:31099800-31099950	Hela-S3	cervix:	n/a	chr12:31099840-31099858 chr12:31099835-31099856 chr12:31099817-31099826
14	CTCF	chr12:31079360-31079510	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr12:31089050-31089311	MCF-7	breast:	n/a	n/a
16	CTCF	chr12:31099720-31099870	GM12871	blood:	n/a	chr12:31099840-31099858 chr12:31099835-31099856 chr12:31099817-31099826
17	CTCF	chr12:31099802-31099889	HepG2	liver:	n/a	chr12:31099840-31099858 chr12:31099835-31099856 chr12:31099817-31099826
18	CTCF	chr12:31079400-31079550	AG04450	lung:	n/a	n/a
19	CTCF	chr12:31079472-31079555	IMR90	lung:	n/a	chr12:31079543-31079551
20	CTCF	chr12:31092752-31092824	GM10248	blood:	n/a	n/a
21	CTCF	chr12:31099800-31099950	HMF	breast:	n/a	chr12:31099840-31099858 chr12:31099835-31099856 chr12:31099817-31099826
22	CTCF	chr12:31089080-31089230	AG09309	skin:	n/a	n/a
23	CTCF	chr12:31079340-31079490	BJ	skin:	n/a	n/a
24	CTCF	chr12:31089020-31089170	AG10803	skin:	n/a	n/a
25	CTCF	chr12:31089060-31089210	AG10803	skin:	n/a	n/a
26	CTCF	chr12:31089080-31089230	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr12:31079360-31079510	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr12:31079380-31079530	AG09319	gingival:	n/a	n/a
29	CTCF	chr12:31089100-31089250	AG09319	gingival:	n/a	n/a
30	CTCF	chr12:31079160-31079310	HAc	cerebellar:	n/a	n/a
31	CTCF	chr12:31089086-31089128	GM13976	blood:	n/a	n/a
32	CTCF	chr12:31099812-31099905	K562	blood:	n/a	chr12:31099840-31099858 chr12:31099835-31099856 chr12:31099817-31099826
33	CTCF	chr12:31099580-31099730	NHLF	lung:	n/a	n/a
34	CTCF	chr12:31089100-31089250	HMF	breast:	n/a	n/a
35	CTCF	chr12:31099785-31099903	H1-hESC	embryonic stem cell:	n/a	chr12:31099840-31099858 chr12:31099835-31099856 chr12:31099817-31099826
36	CTCF	chr12:31089103-31089242	LNCaP	prostate:	n/a	n/a
37	CTCF	chr12:31078001-31078077	GM13976	blood:	n/a	n/a
38	CTCF	chr12:31099760-31099910	HepG2	liver:	n/a	chr12:31099840-31099858 chr12:31099835-31099856 chr12:31099817-31099826
39	CTCF	chr12:31099781-31099906	K562	blood:	n/a	chr12:31099840-31099858 chr12:31099835-31099856 chr12:31099817-31099826
40	CTCF	chr12:31099743-31099939	K562	blood:	n/a	chr12:31099840-31099858 chr12:31099835-31099856 chr12:31099817-31099826
41	CTCF	chr12:31079380-31079530	HAc	cerebellar:	n/a	n/a
42	CTCF	chr12:31095340-31095490	Caco-2	colon:	n/a	n/a
43	CTCF	chr12:31079440-31079590	AG04449	skin:	n/a	chr12:31079543-31079551
44	CTCF	chr12:31089120-31089229	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr12:31099780-31099930	WERI-Rb-1	eye:	n/a	chr12:31099840-31099858 chr12:31099835-31099856 chr12:31099817-31099826
46	CTCF	chr12:31089060-31089210	AG04449	skin:	n/a	n/a
47	CTCF	chr12:31079320-31079470	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr12:31099740-31099890	WERI-Rb-1	eye:	n/a	chr12:31099840-31099858 chr12:31099835-31099856 chr12:31099817-31099826
49	CTCF	chr12:31089060-31089210	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr12:31089145-31089194	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31079583-31079633	HMEC	breast:	n/a
2	chr12:31080052-31080102	PFSK-1	brain:	n/a
3	chr12:31083391-31083441	K562	blood:	n/a
4	chr12:31079694-31079744	HepG2	liver:	n/a
5	chr12:31083391-31083441	GM06990	blood:	n/a
6	chr12:31078979-31079029	H1-hESC	embryonic stem cell:	embryo
7	chr12:31080052-31080102	AG09319	gingival:	n/a
8	chr12:31079406-31079456	K562	blood:	n/a
9	chr12:31079406-31079456	AoSMC	blood vessel:	n/a
10	chr12:31075924-31075974	H1-hESC	embryonic stem cell:	embryo
11	chr12:31079406-31079456	HRPEpiC	eye:	n/a
12	chr12:31078790-31078840	NHDF-neo	bronchial:	n/a
13	chr12:31080052-31080102	LNCaP	prostate:	n/a
14	chr12:31083391-31083441	T-47D	breast:	n/a
15	chr12:31078979-31079029	AG10803	skin:	n/a
16	chr12:31078790-31078840	IMR90	lung:	fetal
17	chr12:31078979-31079029	HL-60	blood:	n/a
18	chr12:31075924-31075974	A549	lung:	n/a
19	chr12:31079583-31079633	NT2-D1	testis:	n/a
20	chr12:31080052-31080102	HUVEC	blood vessel:	n/a
21	chr12:31080052-31080102	HAEpiC	amniotic membrane:	n/a
22	chr12:31079406-31079456	HEK293	kidney:	embryo
23	chr12:31078790-31078840	GM12878	blood:	n/a
24	chr12:31079583-31079633	Jurkat	blood:	n/a
25	chr12:31079694-31079744	NT2-D1	testis:	n/a
26	chr12:31079583-31079633	LNCaP	prostate:	n/a
27	chr12:31078979-31079029	HEK293	kidney:	embryo
28	chr12:31079406-31079456	Hela-S3	cervix:	n/a
29	chr12:31078790-31078840	NHBE	bronchial:	n/a
30	chr12:31078790-31078840	ovcar-3	ovarian:	n/a
31	chr12:31079694-31079744	MCF-7	breast:	n/a
32	chr12:31078979-31079029	ProgFib	skin:	n/a
33	chr12:31079406-31079456	ProgFib	skin:	n/a
34	chr12:31079583-31079633	HIPEpiC	eye:	n/a
35	chr12:31079406-31079456	MCF-7	breast:	n/a
36	chr12:31078790-31078840	ECC-1	luminal epithelium:	n/a
37	chr12:31079694-31079744	GM19239	blood:	n/a
38	chr12:31078790-31078840	HL-60	blood:	n/a
39	chr12:31083391-31083441	HCM	heart:	n/a
40	chr12:31083391-31083441	AoSMC	blood vessel:	n/a
41	chr12:31075924-31075974	Hepatocyte	liver:	n/a
42	chr12:31079694-31079744	AG09309	skin:	n/a
43	chr12:31075924-31075974	ECC-1	luminal epithelium:	n/a
44	chr12:31075924-31075974	SKMC	muscle:	n/a
45	chr12:31079694-31079744	A549	lung:	n/a
46	chr12:31080052-31080102	MCF10A-Er-Src	breast:	n/a
47	chr12:31079406-31079456	HCPEpiC	choroid plexus:	n/a
48	chr12:31079583-31079633	HPAEpiC	pulmonary alveolar:	n/a
49	chr12:31075924-31075974	NHDF-neo	bronchial:	n/a
50	chr12:31075924-31075974	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:31063874..31066002-chr12:31083561..31086374,2	MCF-7	breast:
2	chr12:31068113..31070208-chr12:31087806..31090681,2	K562	blood:
3	chr12:31004147..31004726-chr12:31088536..31089374,2	MCF-7	breast:
4	chr12:31086101..31088564-chr12:31089320..31090867,2	K562	blood:
5	chr12:31082310..31084451-chr12:31104159..31107270,3	MCF-7	breast:
6	chr12:31070913..31073527-chr12:31081618..31083991,3	MCF-7	breast:
7	chr12:31068113..31070208-chr12:31087806..31090681,2	K562	blood:
8	chr12:31086101..31088564-chr12:31089320..31090867,2	K562	blood:
9	chr12:31063762..31066653-chr12:31068189..31070611,2	K562	blood:
10	chr12:31070913..31073527-chr12:31081618..31083991,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAPRIN2-5	chr12:31073397-31074125	NONHSAT027523
2	lnc-CAPRIN2-5	chr12:31076691-31076831	NONHSAT027523

Variant related genes	Relation type
TSPAN11	TF binding region
TSPAN11	CpG island

Extended variants
information (count: 1095 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1095 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79840124	chr12:31069125-31069126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538635576	chr12:31069141-31069142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553754434	chr12:31069153-31069154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs33220	chr12:31069217-31069218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141719299	chr12:31069236-31069237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143300413	chr12:31069267-31069268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556030777	chr12:31069269-31069270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574198603	chr12:31069302-31069303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544443600	chr12:31069319-31069320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563007610	chr12:31069365-31069366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577997919	chr12:31069369-31069370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35266787	chr12:31069385-31069386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147540614	chr12:31069419-31069420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560102984	chr12:31069422-31069423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375132007	chr12:31069424-31069425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527612961	chr12:31069429-31069430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548847477	chr12:31069438-31069439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560823164	chr12:31069464-31069465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531552642	chr12:31069479-31069480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549671716	chr12:31069506-31069507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191104225	chr12:31069510-31069511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs33221	chr12:31069521-31069522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538353684	chr12:31069532-31069533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547457719	chr12:31069533-31069534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571383247	chr12:31069547-31069548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs367848568	chr12:31069549-31069550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565664991	chr12:31069554-31069555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs57610876	chr12:31069555-31069556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556110558	chr12:31069561-31069562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148500886	chr12:31069601-31069602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538435476	chr12:31069614-31069615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551435609	chr12:31069676-31069677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10843858	chr12:31069683-31069684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183287268	chr12:31069776-31069777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545080624	chr12:31069787-31069788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7302052	chr12:31069897-31069898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113142153	chr12:31069909-31069910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542580718	chr12:31069913-31069914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527517867	chr12:31069942-31069943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs33222	chr12:31070020-31070021	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
41	rs187533110	chr12:31070029-31070030	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs549996557	chr12:31070038-31070039	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs113768436	chr12:31070046-31070047	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs564922919	chr12:31070052-31070053	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs532279726	chr12:31070060-31070061	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs370284108	chr12:31070093-31070094	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs547493995	chr12:31070106-31070107	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs192002411	chr12:31070111-31070112	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs536262200	chr12:31070160-31070161	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs548160773	chr12:31070163-31070164	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
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
Ewing''s sarcoma	17952124	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
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31063000-31069800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr12:31063200-31069600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr12:31064200-31069800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr12:31068200-31069400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:31069400-31069600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:31069400-31071000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr12:31069600-31069800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr12:31069600-31071000	Enhancers	H1 Cell Line	embryonic stem cell
9	chr12:31069800-31070000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr12:31069800-31070400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:31069800-31070400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr12:31069800-31070400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr12:31070000-31070400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr12:31075600-31076400	Enhancers	Right Atrium	heart
15	chr12:31076000-31076600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr12:31076200-31076400	Enhancers	Left Ventricle	heart
17	chr12:31076400-31079000	Weak transcription	Right Atrium	heart
18	chr12:31076600-31078800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr12:31077800-31079000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:31077800-31079000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr12:31078000-31078600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
22	chr12:31078000-31079000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:31078200-31079000	Bivalent Enhancer	Fetal Muscle Leg	muscle
24	chr12:31078400-31078600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
25	chr12:31078400-31078600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr12:31078400-31078600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
27	chr12:31078400-31078600	Enhancers	Brain Anterior Caudate	brain
28	chr12:31078400-31078600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
29	chr12:31078400-31078800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr12:31078400-31078800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
31	chr12:31078400-31079000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr12:31078400-31079000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr12:31078400-31079200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
34	chr12:31078400-31080000	Enhancers	Fetal Heart	heart
35	chr12:31078600-31078800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
36	chr12:31078600-31078800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
37	chr12:31078600-31078800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr12:31078600-31078800	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr12:31078600-31078800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
40	chr12:31078600-31078800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
41	chr12:31078600-31078800	Enhancers	Brain Cingulate Gyrus	brain
42	chr12:31078600-31078800	Enhancers	Brain Germinal Matrix	brain
43	chr12:31078600-31078800	Enhancers	Fetal Brain Female	brain
44	chr12:31078600-31078800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
45	chr12:31078600-31078800	Bivalent/Poised TSS	Hela-S3	cervix
46	chr12:31078600-31079000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:31078600-31079000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr12:31078600-31079000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr12:31078600-31079000	Bivalent Enhancer	Brain Anterior Caudate	brain
50	chr12:31078600-31079000	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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