Variant report

Variant	nsv469472
Chromosome Location	chr12:74651797-74690292
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:260)
CpG islands
(count:550)
Chromatin interactive
region (count:16)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:74656460-74656499	K562	blood:	n/a	n/a
2	ARID3A	chr12:74686394-74686740	K562	blood:	n/a	n/a
3	ARID3A	chr12:74677511-74677734	K562	blood:	n/a	n/a
4	ATF1	chr12:74686375-74686953	K562	blood:	n/a	n/a
5	BHLHE40	chr12:74653397-74653481	HepG2	liver:	n/a	n/a
6	BHLHE40	chr12:74686194-74687073	K562	blood:	n/a	n/a
7	BHLHE40	chr12:74687322-74688058	K562	blood:	n/a	n/a
8	CBX3	chr12:74686301-74686730	K562	blood:	n/a	n/a
9	CBX3	chr12:74687157-74687922	K562	blood:	n/a	n/a
10	CBX3	chr12:74686218-74687007	K562	blood:	n/a	n/a
11	CCNT2	chr12:74686228-74686909	K562	blood:	n/a	chr12:74686489-74686509
12	CEBPB	chr12:74658158-74658471	H1-hESC	embryonic stem cell:	n/a	chr12:74658331-74658342
13	CEBPB	chr12:74679616-74679818	A549	lung:	n/a	n/a
14	CEBPB	chr12:74686227-74686696	K562	blood:	n/a	n/a
15	CEBPB	chr12:74658206-74658517	HepG2	liver:	n/a	chr12:74658331-74658342
16	CEBPB	chr12:74680258-74680372	K562	blood:	n/a	n/a
17	CEBPB	chr12:74658328-74658404	K562	blood:	n/a	chr12:74658331-74658342
18	CEBPB	chr12:74658271-74658476	A549	lung:	n/a	chr12:74658331-74658342
19	CEBPB	chr12:74686352-74686893	K562	blood:	n/a	n/a
20	CEBPB	chr12:74658260-74658513	IMR90	lung:	n/a	chr12:74658331-74658342
21	CEBPD	chr12:74686172-74686749	K562	blood:	n/a	n/a
22	CHD2	chr12:74687474-74687667	K562	blood:	n/a	n/a
23	CHD2	chr12:74687891-74688044	K562	blood:	n/a	n/a
24	CHD2	chr12:74686188-74686982	K562	blood:	n/a	n/a
25	CTCF	chr12:74662760-74662910	A549	lung:	n/a	n/a
26	CTCF	chr12:74674800-74674950	MCF-7	breast:	n/a	n/a
27	CTCF	chr12:74662872-74662996	GM12878	blood:	n/a	n/a
28	CTCF	chr12:74663828-74664009	A549	lung:	n/a	n/a
29	CTCF	chr12:74663867-74663955	LNCaP	prostate:	n/a	n/a
30	CTCF	chr12:74662860-74663010	NHEK	skin:	n/a	n/a
31	CTCF	chr12:74662860-74663010	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr12:74686260-74686410	K562	blood:	n/a	n/a
33	CTCF	chr12:74662880-74663030	HEK293	kidney:	n/a	n/a
34	CTCF	chr12:74662913-74662973	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:74663775-74664122	A549	lung:	n/a	n/a
36	CTCF	chr12:74667770-74667820	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr12:74663862-74663941	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:74662920-74663004	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr12:74686287-74686725	K562	blood:	n/a	chr12:74686694-74686707
40	CTCF	chr12:74663720-74663870	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:74674840-74674990	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:74662892-74662955	LNCaP	prostate:	n/a	n/a
43	CTCF	chr12:74662840-74662990	HMEC	breast:	n/a	n/a
44	CTCF	chr12:74662798-74663009	A549	lung:	n/a	n/a
45	CTCF	chr12:74662914-74662999	A549	lung:	n/a	n/a
46	CTCF	chr12:74663786-74664025	A549	lung:	n/a	n/a
47	CTCF	chr12:74662899-74663002	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:74662760-74662910	HMEC	breast:	n/a	n/a
49	CTCF	chr12:74663868-74663990	LNCaP	prostate:	n/a	n/a
50	CTCF	chr12:74660122-74660137	Spleen_OC	spleen:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74686282-74686332	HCPEpiC	choroid plexus:	n/a
2	chr12:74686282-74686332	HCPEpiC	choroid plexus:	n/a
3	chr12:74686282-74686332	K562	blood:	n/a
4	chr12:74687852-74687902	SK-N-MC	brain:	n/a
5	chr12:74686423-74686473	GM06990	blood:	n/a
6	chr12:74686367-74686417	HIPEpiC	eye:	n/a
7	chr12:74687852-74687902	HPAEpiC	pulmonary alveolar:	n/a
8	chr12:74687852-74687902	AoSMC	blood vessel:	n/a
9	chr12:74686423-74686473	HUVEC	blood vessel:	n/a
10	chr12:74686430-74686480	HCM	heart:	n/a
11	chr12:74687852-74687902	NT2-D1	testis:	n/a
12	chr12:74686367-74686417	HCPEpiC	choroid plexus:	n/a
13	chr12:74686282-74686332	Hela-S3	cervix:	n/a
14	chr12:74686411-74686461	NHBE	bronchial:	n/a
15	chr12:74686367-74686417	GM12878	blood:	n/a
16	chr12:74686423-74686473	ECC-1	luminal epithelium:	n/a
17	chr12:74686423-74686473	PANC-1	pancreas:	n/a
18	chr12:74687807-74687857	IMR90	lung:	fetal
19	chr12:74688000-74688050	HEEpiC	esophagus:	n/a
20	chr12:74687404-74687454	HIPEpiC	eye:	n/a
21	chr12:74686423-74686473	GM12878	blood:	n/a
22	chr12:74686411-74686461	HCPEpiC	choroid plexus:	n/a
23	chr12:74686430-74686480	NH-A	brain:	n/a
24	chr12:74687404-74687454	BE2_C	brain:	n/a
25	chr12:74688000-74688050	SAEC	small airway:	n/a
26	chr12:74686423-74686473	Caco-2	colon:	n/a
27	chr12:74687404-74687454	PrEC	prostate:	n/a
28	chr12:74686282-74686332	HUVEC	blood vessel:	n/a
29	chr12:74686367-74686417	SK-N-MC	brain:	n/a
30	chr12:74687807-74687857	BJ	skin:	n/a
31	chr12:74687852-74687902	HAEpiC	amniotic membrane:	n/a
32	chr12:74687404-74687454	GM12878	blood:	n/a
33	chr12:74686367-74686417	IMR90	lung:	fetal
34	chr12:74686423-74686473	U87	brain:	n/a
35	chr12:74686367-74686417	NB4	blood:	n/a
36	chr12:74686282-74686332	LNCaP	prostate:	n/a
37	chr12:74688000-74688050	ProgFib	skin:	n/a
38	chr12:74686411-74686461	SKMC	muscle:	n/a
39	chr12:74687852-74687902	HUVEC	blood vessel:	n/a
40	chr12:74687404-74687454	T-47D	breast:	n/a
41	chr12:74686367-74686417	NH-A	brain:	n/a
42	chr12:74686411-74686461	IMR90	lung:	fetal
43	chr12:74687852-74687902	NB4	blood:	n/a
44	chr12:74687404-74687454	K562	blood:	n/a
45	chr12:74686367-74686417	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:74686367-74686417	SK-N-SH_RA	brain:	n/a
47	chr12:74686282-74686332	NHDF-neo	bronchial:	n/a
48	chr12:74686282-74686332	BJ	skin:	n/a
49	chr12:74686367-74686417	Caco-2	colon:	n/a
50	chr12:74688000-74688050	MCF-7	breast:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:74685342..74687615-chr12:74688335..74689861,2	K562	blood:
2	chr12:74687125..74689371-chr12:74929648..74931476,2	K562	blood:
3	chr12:74683740..74685933-chr12:74788608..74790315,2	K562	blood:
4	chr12:74644729..74646901-chr12:74673133..74675574,2	K562	blood:
5	chr12:74636496..74638215-chr12:74687391..74689120,2	K562	blood:
6	chr12:74666319..74668697-chr12:74685247..74688031,2	K562	blood:
7	chr12:74651832..74654343-chr12:74685350..74686899,2	K562	blood:
8	chr12:74683373..74686280-chr12:74686483..74688021,2	K562	blood:
9	chr12:74665740..74669751-chr12:74671344..74674608,3	K562	blood:
10	chr12:74686465..74688529-chr12:74932040..74934610,2	K562	blood:
11	chr12:74573561..74575455-chr12:74654364..74657073,2	K562	blood:
12	chr12:74682181..74684758-chr12:74690974..74692662,2	MCF-7	breast:
13	chr12:74685273..74687304-chrX:26574250..26577248,2	K562	blood:
14	chr12:74683373..74686280-chr12:74686483..74688021,2	K562	blood:
15	chr12:74663321..74665597-chr12:74668555..74670955,2	K562	blood:
16	chr12:74563726..74565313-chr12:74683248..74684953,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNC2-2	chr12:74678816-74678873	ENSG00000251138
2	lnc-KCNC2-2	chr12:74686095-74686314	ENSG00000251138
3	lnc-KCNC2-2	chr12:74679640-74679726	ENSG00000251138
4	lnc-KCNC2-2	chr12:74679478-74679726	ENSG00000251138
5	lnc-KCNC2-3	chr12:74677374-74677449	ENSG00000257183.1
6	lnc-KCNC2-3	chr12:74663089-74663233	ENSG00000257183.1
7	lnc-ATXN7L3B-5	chr12:74668732-74669011	NONHSAT029501

No data

Variant related genes	Relation type
ENSG00000257183	TF binding region
ENSG00000257113	TF binding region
ENSG00000257364	TF binding region
ENSG00000251138	TF binding region
ENSG00000257183	CpG island
ENSG00000257113	CpG island
ENSG00000257364	CpG island
ENSG00000251138	CpG island
ENSG00000230265	chromatin interactions
ENSG00000259849	chromatin interactions
ENSG00000251138	chromatin interactions
ENSG00000257113	chromatin interactions
ENSG00000257386	chromatin interactions
ENSG00000257364	chromatin interactions
ENSG00000258320	chromatin interactions
RRAS	miRNA target sites
DNMT1	miRNA target sites
DYNLL2	miRNA target sites
PROSC	miRNA target sites

Extended variants
information (count: 1515 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1515 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7294453	chr12:74651797-74651798	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112379105	chr12:74651806-74651807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143974937	chr12:74651814-74651815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536534285	chr12:74651839-74651840	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs74105247	chr12:74651878-74651879	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs373994123	chr12:74651975-74651976	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs147332912	chr12:74651982-74651983	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs506666	chr12:74652026-74652027	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs624394	chr12:74652047-74652048	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543568664	chr12:74652056-74652057	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs565678613	chr12:74652172-74652173	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs370694579	chr12:74652178-74652179	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs117470014	chr12:74652195-74652196	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs112258360	chr12:74652206-74652207	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs1522126	chr12:74652241-74652242	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs575040177	chr12:74652247-74652248	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs374872606	chr12:74652248-74652249	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs509230	chr12:74652260-74652261	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs111532514	chr12:74652274-74652275	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs576735976	chr12:74652432-74652433	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs545500228	chr12:74652437-74652438	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs528248234	chr12:74652440-74652441	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs34573938	chr12:74652514-74652515	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs551178744	chr12:74652546-74652547	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs140584198	chr12:74652560-74652561	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs372963536	chr12:74652667-74652668	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs571143204	chr12:74652676-74652677	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs67630387	chr12:74652734-74652735	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs548348434	chr12:74652769-74652770	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs550700949	chr12:74652784-74652785	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs141016168	chr12:74652788-74652789	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs536652829	chr12:74652795-74652796	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs553363217	chr12:74652816-74652817	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs567166156	chr12:74652841-74652842	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs576213094	chr12:74652855-74652856	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs17113256	chr12:74652882-74652883	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559171417	chr12:74652915-74652916	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs568172015	chr12:74652925-74652926	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs367621174	chr12:74652997-74652998	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs537095936	chr12:74653000-74653001	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs575955132	chr12:74653057-74653058	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs543536271	chr12:74653118-74653119	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs557104003	chr12:74653123-74653124	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs143041684	chr12:74653205-74653206	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs542632049	chr12:74653261-74653262	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559351304	chr12:74653276-74653277	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs528372036	chr12:74653291-74653292	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs544930982	chr12:74653307-74653308	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs113675808	chr12:74653361-74653362	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs564735329	chr12:74653453-74653454	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	20409316	CNVD

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74636600-74678000	Weak transcription	K562	blood
2	chr12:74652200-74652400	Enhancers	Brain Cingulate Gyrus	brain
3	chr12:74652200-74652400	Enhancers	Brain Hippocampus Middle	brain
4	chr12:74652200-74653600	Enhancers	Brain Substantia Nigra	brain
5	chr12:74652400-74653400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr12:74652600-74653200	Weak transcription	Brain Hippocampus Middle	brain
7	chr12:74652800-74653400	Enhancers	Fetal Heart	heart
8	chr12:74652800-74653600	Enhancers	A549	lung
9	chr12:74653000-74653600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr12:74653200-74653600	Enhancers	Brain Hippocampus Middle	brain
11	chr12:74653400-74653600	Flanking Active TSS	Brain Cingulate Gyrus	brain
12	chr12:74653400-74653800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr12:74653400-74653800	Enhancers	Brain Anterior Caudate	brain
14	chr12:74653400-74653800	Flanking Active TSS	Fetal Heart	heart
15	chr12:74653600-74653800	Active TSS	Brain Cingulate Gyrus	brain
16	chr12:74653600-74653800	Flanking Active TSS	Brain Hippocampus Middle	brain
17	chr12:74653600-74657600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr12:74653800-74654600	Enhancers	Fetal Heart	heart
19	chr12:74654400-74654600	Enhancers	Placenta	Placenta
20	chr12:74654600-74657600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:74657600-74658000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr12:74657600-74658000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr12:74657600-74658400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:74657800-74658400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr12:74658200-74658800	Enhancers	H1 Cell Line	embryonic stem cell
26	chr12:74658400-74658600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr12:74658400-74658600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:74658600-74658800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr12:74658600-74661200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr12:74661200-74661600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr12:74661200-74661600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr12:74661200-74662000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr12:74661200-74662000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr12:74661600-74662600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:74662000-74664600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr12:74662800-74663000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr12:74664000-74664200	Enhancers	Lung	lung
38	chr12:74674000-74674800	Enhancers	Liver	Liver
39	chr12:74674800-74676200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:74675000-74676000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:74675200-74676000	Enhancers	HMEC	breast
42	chr12:74676000-74679000	Weak transcription	HMEC	breast
43	chr12:74676200-74679200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr12:74678000-74678600	Genic enhancers	K562	blood
45	chr12:74678600-74678800	Strong transcription	K562	blood
46	chr12:74678800-74679400	Weak transcription	K562	blood
47	chr12:74679000-74679200	Enhancers	HMEC	breast
48	chr12:74679000-74679400	Enhancers	Placenta	Placenta
49	chr12:74679200-74679600	Weak transcription	HMEC	breast
50	chr12:74679200-74680000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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