Variant report

Variant	esv2422282
Chromosome Location	chr12:31221053-31274514
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	ARID3A	chr12:31227278-31227505	K562	blood:	n/a	n/a
2	ARID3A	chr12:31226612-31226780	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:31227121-31227652	HepG2	liver:	n/a	n/a
4	ATF1	chr12:31267437-31267611	K562	blood:	n/a	n/a
5	ATF1	chr12:31230204-31230267	K562	blood:	n/a	n/a
6	ATF2	chr12:31270089-31270375	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr12:31226662-31226898	K562	blood:	n/a	n/a
8	BACH1	chr12:31270094-31270475	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr12:31226535-31226812	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
11	BATF	chr12:31226544-31227607	GM12878	blood:	n/a	n/a
12	BATF	chr12:31228050-31228506	GM12878	blood:	n/a	chr12:31228339-31228347
13	BATF	chr12:31227825-31228526	GM12878	blood:	n/a	chr12:31228339-31228347
14	BATF	chr12:31233393-31233591	GM12878	blood:	n/a	n/a
15	BATF	chr12:31233397-31233563	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:31228135-31228506	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:31226719-31227117	GM12878	blood:	n/a	chr12:31226785-31226794 chr12:31227056-31227065
18	BCL11A	chr12:31226764-31227047	GM12878	blood:	n/a	chr12:31226785-31226794
19	BCL11A	chr12:31227413-31227974	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
20	BCL11A	chr12:31228004-31228492	GM12878	blood:	n/a	n/a
21	BCL11A	chr12:31227467-31227641	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
22	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
23	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:31270186-31270438	K562	blood:	n/a	n/a
26	BHLHE40	chr12:31270127-31270331	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:31227096-31227339	K562	blood:	n/a	chr12:31227176-31227192
28	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:31226599-31226889	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
31	BHLHE40	chr12:31227101-31227187	GM12878	blood:	n/a	n/a
32	BHLHE40	chr12:31226533-31226888	K562	blood:	n/a	n/a
33	BRCA1	chr12:31226630-31226830	GM12878	blood:	n/a	n/a
34	BRCA1	chr12:31270178-31270208	GM12878	blood:	n/a	n/a
35	BRCA1	chr12:31226555-31227323	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr12:31226185-31227769	K562	blood:	n/a	n/a
37	CBX3	chr12:31224793-31225171	K562	blood:	n/a	n/a
38	CEBPB	chr12:31268138-31268370	H1-hESC	embryonic stem cell:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
39	CEBPB	chr12:31268038-31268391	IMR90	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
40	CEBPB	chr12:31268034-31268387	A549	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
41	CEBPB	chr12:31268025-31268366	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
42	CEBPB	chr12:31268131-31268303	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
43	CEBPB	chr12:31268032-31268392	HepG2	liver:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
44	CEBPB	chr12:31232555-31232661	HepG2	liver:	n/a	n/a
45	CEBPB	chr12:31231821-31232014	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr12:31268200-31268216	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr12:31226603-31227301	Hela-S3	cervix:	n/a	chr12:31227015-31227027
48	CEBPB	chr12:31226508-31227197	GM12878	blood:	n/a	chr12:31227015-31227027
49	CEBPD	chr12:31226951-31227517	K562	blood:	n/a	n/a
50	CEBPD	chr12:31226472-31226934	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31255279-31255329	A549	lung:	n/a
2	chr12:31255279-31255329	A549	lung:	n/a
3	chr12:31233201-31233251	HEEpiC	esophagus:	n/a
4	chr12:31255279-31255329	MCF-7	breast:	n/a
5	chr12:31271783-31271833	AG09319	gingival:	n/a
6	chr12:31257362-31257412	MCF10A-Er-Src	breast:	n/a
7	chr12:31227271-31227321	NH-A	brain:	n/a
8	chr12:31230936-31230986	AG10803	skin:	n/a
9	chr12:31272119-31272169	BJ	skin:	n/a
10	chr12:31226952-31227002	HMEC	breast:	n/a
11	chr12:31226825-31226875	HUVEC	blood vessel:	n/a
12	chr12:31272119-31272169	HIPEpiC	eye:	n/a
13	chr12:31226632-31226682	CMK	blood:	n/a
14	chr12:31254007-31254057	PrEC	prostate:	n/a
15	chr12:31272865-31272915	U87	brain:	n/a
16	chr12:31272114-31272164	U87	brain:	n/a
17	chr12:31241496-31241546	SKMC	muscle:	n/a
18	chr12:31272119-31272169	GM12892	blood:	n/a
19	chr12:31230936-31230986	NH-A	brain:	n/a
20	chr12:31226714-31226764	NHBE	bronchial:	n/a
21	chr12:31272114-31272164	HPAEpiC	pulmonary alveolar:	n/a
22	chr12:31230936-31230986	GM19239	blood:	n/a
23	chr12:31271429-31271479	NT2-D1	testis:	n/a
24	chr12:31226536-31226586	HMEC	breast:	n/a
25	chr12:31254036-31254086	NHBE	bronchial:	n/a
26	chr12:31271429-31271479	HRPEpiC	eye:	n/a
27	chr12:31223310-31223360	NHDF-neo	bronchial:	n/a
28	chr12:31257362-31257412	HEEpiC	esophagus:	n/a
29	chr12:31226718-31226768	HMEC	breast:	n/a
30	chr12:31226632-31226682	HMEC	breast:	n/a
31	chr12:31256838-31256888	HAEpiC	amniotic membrane:	n/a
32	chr12:31226801-31226851	NHBE	bronchial:	n/a
33	chr12:31226622-31226672	NH-A	brain:	n/a
34	chr12:31226825-31226875	ProgFib	skin:	n/a
35	chr12:31271783-31271833	SK-N-SH_RA	brain:	n/a
36	chr12:31271783-31271833	GM12892	blood:	n/a
37	chr12:31254007-31254057	T-47D	breast:	n/a
38	chr12:31271429-31271479	SK-N-SH	brain:	n/a
39	chr12:31226718-31226768	BE2_C	brain:	n/a
40	chr12:31271429-31271479	SAEC	small airway:	n/a
41	chr12:31226714-31226764	HEEpiC	esophagus:	n/a
42	chr12:31271429-31271479	HEEpiC	esophagus:	n/a
43	chr12:31272114-31272164	HRCEpiC	kidney:	n/a
44	chr12:31226606-31226656	ovcar-3	ovarian:	n/a
45	chr12:31271783-31271833	HRPEpiC	eye:	n/a
46	chr12:31254036-31254086	U87	brain:	n/a
47	chr12:31257362-31257412	SK-N-MC	brain:	n/a
48	chr12:31272112-31272162	SK-N-MC	brain:	n/a
49	chr12:31254036-31254086	SK-N-SH_RA	brain:	n/a
50	chr12:31241496-31241546	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:9435913..9436700-chr12:31226425..31227148,3	HCT-116	colon:
2	chr12:9436173..9436735-chr12:31226434..31227168,3	Hela-S3	cervix:
3	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
4	chr12:31226738..31227630-chr20:47894738..47895520,2	Hela-S3	cervix:
5	chr12:31226022..31227620-chr12:31260408..31262678,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-6	chr12:31269291-31269403	NONHSAT140066
2	lnc-FAM60A-7	chr12:31264627-31264743	NONHSAT027538
3	lnc-FAM60A-7	chr12:31267330-31267397	NONHSAT027538
4	lnc-FAM60A-7	chr12:31265915-31266017	NONHSAT027538
5	lnc-FAM60A-6	chr12:31270354-31270558	NONHSAT140066

Variant related genes	Relation type
DDX11-AS1	TF binding region
ENSG00000177359	TF binding region
ENSG00000270926	TF binding region
ENSG00000212533	TF binding region
DDX11	TF binding region
DDX11-AS1	CpG island
ENSG00000177359	CpG island
ENSG00000270926	CpG island
ENSG00000212533	CpG island
DDX11	CpG island
ENSG00000243517	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000111788	chromatin interactions
ENSG00000177410	chromatin interactions
ENSG00000245614	chromatin interactions
ENSG00000013573	chromatin interactions
ENSG00000209042	chromatin interactions

Extended variants
information (count: 2960 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2960 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369434313	chr12:31221054-31221055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs11051231	chr12:31221072-31221073	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs576487528	chr12:31221073-31221074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143984566	chr12:31221076-31221077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540275225	chr12:31221101-31221102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552664045	chr12:31221149-31221150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189072799	chr12:31221208-31221209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547728259	chr12:31221265-31221266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141030983	chr12:31221305-31221306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542934991	chr12:31221319-31221320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561569934	chr12:31221321-31221322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531808880	chr12:31221344-31221345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181475933	chr12:31221347-31221348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565395674	chr12:31221384-31221385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561624821	chr12:31221423-31221424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185081907	chr12:31221429-31221430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529024184	chr12:31221443-31221444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532624596	chr12:31221445-31221446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11051232	chr12:31221455-31221456	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs34723189	chr12:31221474-31221475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149504925	chr12:31221475-31221476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560376446	chr12:31221477-31221478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565383047	chr12:31221478-31221479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs59932314	chr12:31221498-31221499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs71052455	chr12:31221501-31221502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201560502	chr12:31221504-31221505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562496155	chr12:31221513-31221514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374685024	chr12:31221541-31221542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35516424	chr12:31221560-31221561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73089797	chr12:31221621-31221622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73089802	chr12:31221622-31221623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569888168	chr12:31221645-31221646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138250464	chr12:31221649-31221650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs117463717	chr12:31221652-31221653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367762041	chr12:31221689-31221690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551716502	chr12:31221743-31221744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2543239	chr12:31221767-31221768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536854568	chr12:31221772-31221773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558293663	chr12:31221829-31221830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34481011	chr12:31221863-31221864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs67009918	chr12:31221880-31221881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149580072	chr12:31221897-31221898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534389648	chr12:31221903-31221904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111745017	chr12:31221928-31221929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566622175	chr12:31222025-31222026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552967110	chr12:31222161-31222162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574340635	chr12:31222168-31222169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12425683	chr12:31222178-31222179	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs180929085	chr12:31222188-31222189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111965058	chr12:31222239-31222240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
Lung cancer	18438408	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
Sertoli-cell only syndrome	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1932 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31189800-31225400	Weak transcription	Fetal Stomach	stomach
2	chr12:31210800-31225200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:31219600-31225600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr12:31220400-31221200	Enhancers	HMEC	breast
5	chr12:31220400-31221200	Enhancers	NHEK	skin
6	chr12:31220800-31221400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:31220800-31221600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr12:31221000-31225600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:31221200-31225400	Weak transcription	HMEC	breast
10	chr12:31221200-31225600	Weak transcription	NHEK	skin
11	chr12:31221400-31225600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr12:31221600-31225600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr12:31225000-31225200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr12:31225000-31225200	Enhancers	Dnd41	blood
15	chr12:31225200-31225400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr12:31225200-31225400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:31225200-31225400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:31225200-31225400	Active TSS	Fetal Thymus	thymus
19	chr12:31225200-31225400	Active TSS	Hela-S3	cervix
20	chr12:31225200-31225600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr12:31225200-31225600	Enhancers	HepG2	liver
22	chr12:31225200-31225600	Enhancers	K562	blood
23	chr12:31225200-31225800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr12:31225200-31226200	Flanking Active TSS	Dnd41	blood
25	chr12:31225200-31228000	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr12:31225200-31228400	Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr12:31225200-31228600	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr12:31225400-31225600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:31225400-31225600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr12:31225400-31225600	Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr12:31225400-31225600	Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr12:31225400-31225600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr12:31225400-31225600	Flanking Active TSS	Brain Germinal Matrix	brain
34	chr12:31225400-31225600	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr12:31225400-31225600	Flanking Active TSS	Fetal Thymus	thymus
36	chr12:31225400-31225600	Enhancers	Pancreas	Pancrea
37	chr12:31225400-31225600	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr12:31225400-31225800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
39	chr12:31225400-31225800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr12:31225400-31225800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr12:31225400-31225800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr12:31225400-31225800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr12:31225400-31225800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr12:31225400-31225800	Flanking Active TSS	GM12878-XiMat	blood
45	chr12:31225400-31225800	Flanking Active TSS	HMEC	breast
46	chr12:31225400-31226000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr12:31225400-31226000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:31225400-31226000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr12:31225400-31226000	Enhancers	Fetal Muscle Leg	muscle
50	chr12:31225400-31226000	Enhancers	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links