Variant report

Variant	esv3504374
Chromosome Location	chr12:123186465-123200093
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:88)
CpG islands
(count:366)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:88 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:123198368-123198752	GM12878	blood:	n/a	n/a
2	BATF	chr12:123198415-123198667	GM12878	blood:	n/a	n/a
3	BCL11A	chr12:123198389-123198642	GM12878	blood:	n/a	chr12:123198604-123198613
4	CBX3	chr12:123192855-123193151	K562	blood:	n/a	n/a
5	CEBPB	chr12:123192059-123192377	IMR90	lung:	n/a	chr12:123192205-123192216
6	CEBPB	chr12:123187794-123188089	HepG2	liver:	n/a	n/a
7	CEBPB	chr12:123192177-123192277	Hela-S3	cervix:	n/a	chr12:123192205-123192216
8	CEBPB	chr12:123187869-123188146	A549	lung:	n/a	n/a
9	CEBPB	chr12:123187833-123188233	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:123192198-123192210	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr12:123192061-123192396	A549	lung:	n/a	chr12:123192205-123192216
12	CEBPB	chr12:123192060-123192294	HepG2	liver:	n/a	chr12:123192205-123192216
13	CEBPB	chr12:123194984-123195338	MCF-7	breast:	n/a	n/a
14	E2F4	chr12:123187896-123188134	MCF10A-Er-Src	breast:	n/a	n/a
15	EBF1	chr12:123187949-123188264	GM12878	blood:	n/a	n/a
16	EBF1	chr12:123187913-123188259	GM12878	blood:	n/a	n/a
17	EP300	chr12:123187789-123188123	HepG2	liver:	n/a	n/a
18	FOS	chr12:123187821-123188180	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr12:123187796-123188158	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr12:123187570-123188311	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr12:123187706-123188305	MCF10A-Er-Src	breast:	n/a	n/a
22	FOSL2	chr12:123193878-123194221	HepG2	liver:	n/a	n/a
23	FOSL2	chr12:123198037-123198405	HepG2	liver:	n/a	chr12:123198238-123198246 chr12:123198236-123198247 chr12:123198236-123198248 chr12:123198241-123198248
24	FOXA1	chr12:123187829-123188220	HepG2	liver:	n/a	n/a
25	FOXA1	chr12:123187806-123188302	HepG2	liver:	n/a	n/a
26	FOXA2	chr12:123187936-123188118	HepG2	liver:	n/a	n/a
27	GATA2	chr12:123192789-123193089	K562	blood:	n/a	n/a
28	GATA2	chr12:123194868-123195095	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr12:123194628-123195408	MCF-7	breast:	n/a	n/a
30	GATA3	chr12:123194991-123195209	MCF-7	breast:	n/a	n/a
31	GATA3	chr12:123193377-123193611	T-47D	breast:	n/a	n/a
32	GATA3	chr12:123194897-123195387	MCF-7	breast:	n/a	n/a
33	HDAC2	chr12:123194915-123195367	MCF-7	breast:	n/a	n/a
34	HEY1	chr12:123187714-123188013	HepG2	liver:	n/a	n/a
35	IRF4	chr12:123198054-123198813	GM12878	blood:	n/a	n/a
36	IRF4	chr12:123198309-123198803	GM12878	blood:	n/a	n/a
37	JUND	chr12:123194874-123195301	MCF-7	breast:	n/a	n/a
38	JUND	chr12:123198163-123198298	HepG2	liver:	n/a	chr12:123198238-123198246 chr12:123198236-123198247 chr12:123198236-123198248 chr12:123198241-123198248
39	JUND	chr12:123198141-123198327	HepG2	liver:	n/a	chr12:123198238-123198246 chr12:123198236-123198247 chr12:123198236-123198248 chr12:123198241-123198248
40	MYC	chr12:123187728-123188305	MCF10A-Er-Src	breast:	n/a	n/a
41	MYC	chr12:123187750-123188250	MCF10A-Er-Src	breast:	n/a	n/a
42	NFIC	chr12:123198230-123198801	GM12878	blood:	n/a	n/a
43	NR2F2	chr12:123192809-123193203	K562	blood:	n/a	n/a
44	NR2F2	chr12:123194900-123195374	MCF-7	breast:	n/a	n/a
45	NR2F2	chr12:123194844-123195369	MCF-7	breast:	n/a	n/a
46	PAX5	chr12:123198298-123198672	GM12878	blood:	n/a	chr12:123198604-123198613
47	POLR2A	chr12:123187655-123188092	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr12:123198869-123199054	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr12:123187462-123188263	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr12:123194004-123194048	MCF-7	breast:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123188078-123188128	ovcar-3	ovarian:	n/a
2	chr12:123188078-123188128	GM06990	blood:	n/a
3	chr12:123187073-123187123	GM06990	blood:	n/a
4	chr12:123187073-123187123	H1-hESC	embryonic stem cell:	embryo
5	chr12:123187529-123187579	GM12892	blood:	n/a
6	chr12:123187529-123187579	AG04449	skin:	fetal
7	chr12:123189256-123189306	H1-hESC	embryonic stem cell:	embryo
8	chr12:123187529-123187579	AoSMC	blood vessel:	n/a
9	chr12:123187073-123187123	PrEC	prostate:	n/a
10	chr12:123189236-123189286	AG04450	lung:	fetal
11	chr12:123187529-123187579	MCF-7	breast:	n/a
12	chr12:123189236-123189286	GM12891	blood:	n/a
13	chr12:123189236-123189286	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:123187474-123187524	HRE	kidney:	n/a
15	chr12:123187073-123187123	A549	lung:	n/a
16	chr12:123189236-123189286	AG09319	gingival:	n/a
17	chr12:123187529-123187579	Hela-S3	cervix:	n/a
18	chr12:123188078-123188128	SAEC	small airway:	n/a
19	chr12:123187529-123187579	CMK	blood:	n/a
20	chr12:123188078-123188128	PFSK-1	brain:	n/a
21	chr12:123187073-123187123	GM19239	blood:	n/a
22	chr12:123187474-123187524	HAEpiC	amniotic membrane:	n/a
23	chr12:123189236-123189286	T-47D	breast:	n/a
24	chr12:123189236-123189286	NB4	blood:	n/a
25	chr12:123189256-123189306	PrEC	prostate:	n/a
26	chr12:123187474-123187524	ProgFib	skin:	n/a
27	chr12:123188078-123188128	RPTEC	kidney:	n/a
28	chr12:123187073-123187123	AoSMC	blood vessel:	n/a
29	chr12:123187474-123187524	HCT-116	colon:	n/a
30	chr12:123189256-123189306	AG04450	lung:	fetal
31	chr12:123187073-123187123	SAEC	small airway:	n/a
32	chr12:123189236-123189286	PFSK-1	brain:	n/a
33	chr12:123187474-123187524	AG09309	skin:	n/a
34	chr12:123187529-123187579	NB4	blood:	n/a
35	chr12:123187073-123187123	IMR90	lung:	fetal
36	chr12:123187073-123187123	BE2_C	brain:	n/a
37	chr12:123188078-123188128	HIPEpiC	eye:	n/a
38	chr12:123189256-123189306	AoSMC	blood vessel:	n/a
39	chr12:123189256-123189306	HEEpiC	esophagus:	n/a
40	chr12:123187529-123187579	HCPEpiC	choroid plexus:	n/a
41	chr12:123188078-123188128	AG04450	lung:	fetal
42	chr12:123187073-123187123	AG09319	gingival:	n/a
43	chr12:123189236-123189286	NH-A	brain:	n/a
44	chr12:123187474-123187524	A549	lung:	n/a
45	chr12:123187529-123187579	Caco-2	colon:	n/a
46	chr12:123189236-123189286	SKMC	muscle:	n/a
47	chr12:123187474-123187524	SK-N-SH	brain:	n/a
48	chr12:123187529-123187579	H1-hESC	embryonic stem cell:	embryo
49	chr12:123187073-123187123	GM12891	blood:	n/a
50	chr12:123189236-123189286	MCF-7	breast:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:123186486..123188573-chr12:123199930..123201817,2	MCF-7	breast:
2	chr12:123186486..123188573-chr12:123199930..123201817,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DENR-2	chr12:123199801-123200187	NONHSAT031529
2	lnc-DENR-2	chr12:123198838-123199340	ENSG00000256249
3	lnc-DENR-2	chr12:123200008-123200255	ENSG00000256249

No data

Variant related genes	Relation type
ENSG00000256249	TF binding region
HCAR2	TF binding region
ENSG00000256249	CpG island
HCAR2	CpG island
ENSG00000255398	chromatin interactions
ENSG00000182782	chromatin interactions
LRRC41	miRNA target sites
GALNT11	miRNA target sites

Extended variants
information (count: 705 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:705 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538058928	chr12:123186488-123186489	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549254377	chr12:123186492-123186493	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs67140489	chr12:123186506-123186507	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs567565510	chr12:123186513-123186514	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375378061	chr12:123186524-123186525	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs582452	chr12:123186539-123186540	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs552918434	chr12:123186555-123186556	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs187079814	chr12:123186587-123186588	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs579935	chr12:123186596-123186597	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs76270247	chr12:123186610-123186611	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs79685171	chr12:123186611-123186612	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs202220470	chr12:123186692-123186693	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs143443624	chr12:123186699-123186700	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs200807592	chr12:123186708-123186709	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs200735597	chr12:123186720-123186721	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs470939	chr12:123186730-123186731	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs369377442	chr12:123186734-123186735	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs63475561	chr12:123186741-123186742	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs200253923	chr12:123186744-123186745	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs201579375	chr12:123186747-123186748	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs199966560	chr12:123186748-123186749	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs202231409	chr12:123186749-123186750	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs200856181	chr12:123186757-123186758	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs200247476	chr12:123186769-123186770	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201426235	chr12:123186773-123186774	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148160325	chr12:123186783-123186784	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145934041	chr12:123186795-123186796	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs201282262	chr12:123186799-123186800	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs199511843	chr12:123186810-123186811	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200668464	chr12:123186811-123186812	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs201998198	chr12:123186813-123186814	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs138616040	chr12:123186840-123186841	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200174813	chr12:123186846-123186847	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200716997	chr12:123186847-123186848	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs142025654	chr12:123186850-123186851	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143584617	chr12:123186851-123186852	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs375858825	chr12:123186857-123186858	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200898743	chr12:123186858-123186859	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs2454727	chr12:123186880-123186881	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs7314976	chr12:123186900-123186901	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201042656	chr12:123186919-123186920	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs202219060	chr12:123186958-123186959	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs532420349	chr12:123186961-123186962	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs200312833	chr12:123186973-123186974	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs201479596	chr12:123186978-123186979	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551015732	chr12:123186999-123187000	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs202067823	chr12:123187006-123187007	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs200261814	chr12:123187011-123187012	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs201389637	chr12:123187018-123187019	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs199788788	chr12:123187019-123187020	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123166600-123187800	Weak transcription	A549	lung
2	chr12:123174000-123199800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:123184000-123188800	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr12:123185200-123187200	Active TSS	Esophagus	oesophagus
5	chr12:123185400-123186800	Active TSS	Primary hematopoietic stem cells	blood
6	chr12:123185400-123188200	Active TSS	Primary B cells from cord blood	blood
7	chr12:123185800-123187000	Flanking Active TSS	Adipose Nuclei	Adipose
8	chr12:123186000-123187400	Weak transcription	HMEC	breast
9	chr12:123186000-123188000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:123186000-123188000	Enhancers	Placenta	Placenta
11	chr12:123186000-123188200	Enhancers	NHEK	skin
12	chr12:123186000-123188600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr12:123186000-123188600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr12:123186200-123186600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr12:123186200-123186600	Enhancers	Fetal Stomach	stomach
16	chr12:123186200-123186800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr12:123186200-123186800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr12:123186200-123186800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr12:123186200-123186800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:123186400-123186600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr12:123186400-123187400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr12:123186600-123186800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:123186600-123186800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr12:123186800-123187000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr12:123186800-123187400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr12:123186800-123187800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr12:123186800-123188000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr12:123187000-123187200	Enhancers	Adipose Nuclei	Adipose
29	chr12:123187000-123188000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:123187200-123187600	Flanking Active TSS	Esophagus	oesophagus
31	chr12:123187200-123187800	Flanking Active TSS	Adipose Nuclei	Adipose
32	chr12:123187400-123187600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr12:123187400-123187800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr12:123187400-123187800	Enhancers	Spleen	Spleen
35	chr12:123187400-123188000	Enhancers	HMEC	breast
36	chr12:123187400-123188200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr12:123187400-123188600	Enhancers	Hela-S3	cervix
38	chr12:123187600-123187800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr12:123187600-123187800	Active TSS	Esophagus	oesophagus
40	chr12:123187600-123187800	Enhancers	Fetal Thymus	thymus
41	chr12:123187600-123188200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr12:123187600-123188200	Enhancers	HepG2	liver
43	chr12:123187800-123188000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr12:123187800-123188000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr12:123187800-123188000	Enhancers	A549	lung
46	chr12:123187800-123198600	Weak transcription	Adipose Nuclei	Adipose
47	chr12:123188000-123193600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:123188200-123188600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:123188200-123188800	Enhancers	Primary B cells from cord blood	blood
50	chr12:123188200-123192000	Weak transcription	HepG2	liver

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