Variant report

Variant	nsv899165
Chromosome Location	chr12:63545986-63641641
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:406)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:406 , 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	BHLHE40	chr12:63550104-63550132	GM12878	blood:	n/a	n/a
2	BRCA1	chr12:63600642-63601071	Hela-S3	cervix:	n/a	n/a
3	CBX3	chr12:63570065-63570332	K562	blood:	n/a	n/a
4	CEBPB	chr12:63554623-63554689	A549	lung:	n/a	n/a
5	CEBPB	chr12:63624366-63624484	HepG2	liver:	n/a	chr12:63624438-63624449
6	CEBPB	chr12:63577407-63577618	A549	lung:	n/a	chr12:63577475-63577486
7	CEBPB	chr12:63572887-63573147	A549	lung:	n/a	n/a
8	CEBPB	chr12:63577350-63577566	HepG2	liver:	n/a	chr12:63577475-63577486
9	CEBPB	chr12:63625166-63625226	HepG2	liver:	n/a	chr12:63625189-63625200
10	CEBPB	chr12:63569647-63569844	HepG2	liver:	n/a	chr12:63569707-63569718
11	CEBPB	chr12:63569654-63569734	IMR90	lung:	n/a	chr12:63569707-63569718
12	CEBPB	chr12:63607177-63607379	A549	lung:	n/a	n/a
13	CEBPB	chr12:63600261-63601236	MCF-7	breast:	n/a	n/a
14	CEBPB	chr12:63573010-63573086	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:63600785-63601096	A549	lung:	n/a	n/a
16	CEBPB	chr12:63572869-63573101	IMR90	lung:	n/a	n/a
17	CEBPB	chr12:63613516-63613778	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:63616909-63617221	IMR90	lung:	n/a	chr12:63617048-63617059 chr12:63617110-63617121 chr12:63617048-63617061
19	CEBPB	chr12:63572966-63573073	K562	blood:	n/a	n/a
20	CEBPB	chr12:63616923-63617223	HepG2	liver:	n/a	chr12:63617048-63617059 chr12:63617110-63617121 chr12:63617048-63617061
21	CEBPB	chr12:63569649-63569765	A549	lung:	n/a	chr12:63569707-63569718
22	CEBPB	chr12:63600679-63601182	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr12:63613489-63613787	HepG2	liver:	n/a	n/a
24	CEBPB	chr12:63616996-63617194	A549	lung:	n/a	chr12:63617048-63617059 chr12:63617110-63617121 chr12:63617048-63617061
25	CEBPB	chr12:63600554-63601331	MCF-7	breast:	n/a	n/a
26	CHD2	chr12:63600755-63601111	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr12:63545847-63546206	K562	blood:	n/a	chr12:63546025-63546038
28	CTCF	chr12:63545960-63546110	AoAF	blood vessel:	n/a	chr12:63546025-63546038
29	CTCF	chr12:63546718-63546755	LNCaP	prostate:	n/a	n/a
30	CTCF	chr12:63614914-63614921	LNCaP	prostate:	n/a	n/a
31	CTCF	chr12:63545940-63546090	HA-sp	spinal cord:	n/a	chr12:63546025-63546038
32	CTCF	chr12:63545900-63546050	A549	lung:	n/a	chr12:63546025-63546038
33	CTCF	chr12:63545907-63546139	GM19239	blood:	n/a	chr12:63546025-63546038
34	CTCF	chr12:63545940-63546090	AG04449	skin:	n/a	chr12:63546025-63546038
35	CTCF	chr12:63546000-63546150	GM12872	blood:	n/a	chr12:63546025-63546038
36	CTCF	chr12:63545940-63546090	GM12867	blood:	n/a	chr12:63546025-63546038
37	CTCF	chr12:63545940-63546090	HCT-116	colon:	n/a	chr12:63546025-63546038
38	CTCF	chr12:63545940-63546090	NHDF-neo	bronchial:	n/a	chr12:63546025-63546038
39	CTCF	chr12:63545940-63546090	HBMEC	blood vessel:	n/a	chr12:63546025-63546038
40	CTCF	chr12:63545960-63546110	GM12869	blood:	n/a	chr12:63546025-63546038
41	CTCF	chr12:63546720-63546870	HPF	lung:	n/a	n/a
42	CTCF	chr12:63545960-63546110	HVMF	connective:	n/a	chr12:63546025-63546038
43	CTCF	chr12:63545821-63546243	GM12878	blood:	n/a	chr12:63546025-63546038
44	CTCF	chr12:63545960-63546110	HA-sp	spinal cord:	n/a	chr12:63546025-63546038
45	CTCF	chr12:63545960-63546110	HFF-Myc	foreskin:	n/a	chr12:63546025-63546038
46	CTCF	chr12:63545869-63546161	MCF-7	breast:	n/a	chr12:63546025-63546038
47	CTCF	chr12:63545960-63546110	GM12801	blood:	n/a	chr12:63546025-63546038
48	CTCF	chr12:63545901-63546144	GM13977	blood:	n/a	chr12:63546025-63546038
49	CTCF	chr12:63545980-63546130	HCPEpiC	choroid plexus:	n/a	chr12:63546025-63546038
50	CTCF	chr12:63545837-63546203	HepG2	liver:	n/a	chr12:63546025-63546038

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63546263-63546313	HAEpiC	amniotic membrane:	n/a
2	chr12:63547716-63547766	HEK293	kidney:	embryo
3	chr12:63545956-63546006	RPTEC	kidney:	n/a
4	chr12:63546263-63546313	NT2-D1	testis:	n/a
5	chr12:63545956-63546006	Hela-S3	cervix:	n/a
6	chr12:63546263-63546313	AG10803	skin:	n/a
7	chr12:63546263-63546313	SK-N-SH_RA	brain:	n/a
8	chr12:63545956-63546006	PrEC	prostate:	n/a
9	chr12:63545956-63546006	BE2_C	brain:	n/a
10	chr12:63545956-63546006	GM19239	blood:	n/a
11	chr12:63547716-63547766	AG10803	skin:	n/a
12	chr12:63546263-63546313	HCPEpiC	choroid plexus:	n/a
13	chr12:63546263-63546313	Hepatocyte	liver:	n/a
14	chr12:63545956-63546006	ovcar-3	ovarian:	n/a
15	chr12:63546263-63546313	NH-A	brain:	n/a
16	chr12:63546263-63546313	ovcar-3	ovarian:	n/a
17	chr12:63546263-63546313	PFSK-1	brain:	n/a
18	chr12:63545956-63546006	SAEC	small airway:	n/a
19	chr12:63545956-63546006	NB4	blood:	n/a
20	chr12:63546263-63546313	AoSMC	blood vessel:	n/a
21	chr12:63547716-63547766	GM12891	blood:	n/a
22	chr12:63546263-63546313	H1-hESC	embryonic stem cell:	embryo
23	chr12:63545956-63546006	AG04449	skin:	fetal
24	chr12:63545956-63546006	HIPEpiC	eye:	n/a
25	chr12:63546263-63546313	NHDF-neo	bronchial:	n/a
26	chr12:63546263-63546313	IMR90	lung:	fetal
27	chr12:63545956-63546006	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:63545956-63546006	K562	blood:	n/a
29	chr12:63547716-63547766	NT2-D1	testis:	n/a
30	chr12:63545956-63546006	AG04450	lung:	fetal
31	chr12:63545956-63546006	AG09319	gingival:	n/a
32	chr12:63547716-63547766	BE2_C	brain:	n/a
33	chr12:63546263-63546313	HCM	heart:	n/a
34	chr12:63547716-63547766	NB4	blood:	n/a
35	chr12:63547716-63547766	ProgFib	skin:	n/a
36	chr12:63545956-63546006	GM06990	blood:	n/a
37	chr12:63547716-63547766	HRCEpiC	kidney:	n/a
38	chr12:63547716-63547766	HL-60	blood:	n/a
39	chr12:63546263-63546313	GM12892	blood:	n/a
40	chr12:63545956-63546006	PFSK-1	brain:	n/a
41	chr12:63545956-63546006	CMK	blood:	n/a
42	chr12:63546263-63546313	HUVEC	blood vessel:	n/a
43	chr12:63545956-63546006	A549	lung:	n/a
44	chr12:63547716-63547766	CMK	blood:	n/a
45	chr12:63545956-63546006	PANC-1	pancreas:	n/a
46	chr12:63545956-63546006	GM12892	blood:	n/a
47	chr12:63547716-63547766	SK-N-MC	brain:	n/a
48	chr12:63547716-63547766	NHDF-neo	bronchial:	n/a
49	chr12:63547716-63547766	ECC-1	luminal epithelium:	n/a
50	chr12:63547716-63547766	Jurkat	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:63545448..63546470-chr12:63670124..63671316,6	MCF-7	breast:
2	chr12:63632053..63632963-chr5:177630919..177631572,2	Hela-S3	cervix:
3	chr12:63617360..63618250-chr8:143764719..143765546,2	MCF-7	breast:
4	chr12:63545419..63546376-chr12:64195555..64196413,2	MCF-7	breast:
5	chr12:63540258..63542828-chr12:63547028..63548966,2	K562	blood:
6	chr12:63599815..63602634-chr12:63602685..63604731,2	MCF-7	breast:
7	chr12:63535701..63537481-chr12:63551924..63553918,2	MCF-7	breast:
8	chr12:63599815..63602634-chr12:63602685..63604731,2	MCF-7	breast:
9	chr12:63545559..63546473-chr12:63669896..63671149,5	MCF-7	breast:
10	chr12:62996207..62999162-chr12:63547684..63549229,2	MCF-7	breast:
11	chr12:63545428..63546206-chr12:63674883..63675724,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MON2-3	chr12:63547640-63547786	ENSG00000257973.1
2	lnc-TMEM5-5	chr12:63563605-63563746	l_664_chr12:63563604-63657550_brain
3	lnc-TMEM5-5	chr12:63580624-63580735	l_664_chr12:63563604-63657550_brain
4	lnc-MON2-3	chr12:63546261-63546418	ENSG00000257973.1
5	lnc-TMEM5-5	chr12:63563762-63563912	l_664_chr12:63563604-63657550_brain

No data

Variant related genes	Relation type
AVPR1A	TF binding region
AVPR1A	CpG island
ENSG00000199179	chromatin interactions
ENSG00000257354	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000221949	chromatin interactions

Extended variants
information (count: 1104 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1104 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3021528	chr12:63545986-63545987	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558340404	chr12:63546069-63546070	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs75397752	chr12:63546118-63546119	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs552843665	chr12:63546126-63546127	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs538651356	chr12:63546272-63546273	Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs534646833	chr12:63546283-63546284	Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs553726754	chr12:63546418-63546419	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs3021527	chr12:63546527-63546528	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs542679309	chr12:63546563-63546564	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs145801755	chr12:63546570-63546571	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs74097656	chr12:63546618-63546619	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs533542253	chr12:63546634-63546635	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs375701155	chr12:63546642-63546643	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs370003100	chr12:63546646-63546647	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs2738253	chr12:63546709-63546710	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374384141	chr12:63546733-63546734	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs146924260	chr12:63546744-63546745	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs572107783	chr12:63546745-63546746	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs185713771	chr12:63546752-63546753	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs188802530	chr12:63546926-63546927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541782491	chr12:63546945-63546946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561437620	chr12:63547001-63547002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540815301	chr12:63547039-63547040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553811941	chr12:63547053-63547054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147593272	chr12:63547070-63547071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72437702	chr12:63547084-63547085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4026925	chr12:63547092-63547093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375871329	chr12:63547096-63547097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373455174	chr12:63547097-63547098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192185649	chr12:63547100-63547101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140940225	chr12:63547104-63547105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145866023	chr12:63547110-63547111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs3087488	chr12:63547114-63547115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184430878	chr12:63547118-63547119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72112718	chr12:63547124-63547125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141249341	chr12:63547126-63547127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs59810281	chr12:63547134-63547135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113697298	chr12:63547147-63547148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374220840	chr12:63547153-63547154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532627371	chr12:63547154-63547155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570711884	chr12:63547190-63547191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112436328	chr12:63547210-63547211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10877969	chr12:63547239-63547240	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs188481744	chr12:63547240-63547241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559537796	chr12:63547282-63547283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534525824	chr12:63547302-63547303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs3759292	chr12:63547313-63547314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181596816	chr12:63547381-63547382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185773185	chr12:63547384-63547385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372462807	chr12:63547448-63547449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	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	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63543200-63546400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr12:63543600-63546000	Flanking Active TSS	Pancreas	Pancrea
3	chr12:63543600-63546000	Bivalent/Poised TSS	Psoas Muscle	Psoas
4	chr12:63543600-63546000	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
5	chr12:63543800-63546000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr12:63543800-63546000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
7	chr12:63543800-63546000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
8	chr12:63543800-63546000	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
9	chr12:63543800-63546000	Active TSS	Aorta	Aorta
10	chr12:63543800-63546000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
11	chr12:63543800-63546000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
12	chr12:63543800-63546000	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
13	chr12:63543800-63546000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
14	chr12:63543800-63546000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
15	chr12:63543800-63546000	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
16	chr12:63543800-63546200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
17	chr12:63543800-63546200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
18	chr12:63543800-63546800	Flanking Active TSS	Liver	Liver
19	chr12:63544000-63546000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
20	chr12:63544000-63546000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr12:63544000-63546000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
22	chr12:63544000-63546000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr12:63544000-63546000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:63544000-63546000	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr12:63544000-63546000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr12:63544200-63546000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr12:63544200-63546000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
28	chr12:63544200-63546000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr12:63544200-63546000	Bivalent Enhancer	Placenta	Placenta
30	chr12:63544200-63546000	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
31	chr12:63544200-63546000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
32	chr12:63544200-63546000	Flanking Bivalent TSS/Enh	NH-A	brain
33	chr12:63544200-63546200	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
34	chr12:63544200-63546400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
35	chr12:63544200-63546400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
36	chr12:63544400-63546000	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr12:63544400-63546000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
38	chr12:63544400-63546200	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
39	chr12:63544600-63546000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
40	chr12:63544600-63546000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
41	chr12:63544600-63546000	Bivalent/Poised TSS	Ovary	ovary
42	chr12:63544600-63546200	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr12:63545000-63546000	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:63545000-63546000	Flanking Bivalent TSS/Enh	Brain Angular Gyrus	brain
45	chr12:63545000-63546000	Bivalent Enhancer	HMEC	breast
46	chr12:63545000-63546200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
47	chr12:63545200-63546000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:63545200-63546000	Bivalent/Poised TSS	Colonic Mucosa	Colon
49	chr12:63545200-63546000	Bivalent Enhancer	Esophagus	oesophagus
50	chr12:63545200-63546000	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine

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