Variant report

Variant	esv3355177
Chromosome Location	chr14:105261457-105262755
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	BACH1	chr14:105261472-105261498	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr14:105262155-105262338	K562	blood:	n/a	n/a
3	BHLHE40	chr14:105262625-105263043	HepG2	liver:	n/a	n/a
4	BRCA1	chr14:105262685-105262843	HepG2	liver:	n/a	n/a
5	BRCA1	chr14:105262304-105262403	GM12878	blood:	n/a	n/a
6	CCNT2	chr14:105261098-105262537	K562	blood:	n/a	n/a
7	CHD1	chr14:105261172-105261559	GM12878	blood:	n/a	n/a
8	CHD1	chr14:105262711-105262801	GM12878	blood:	n/a	n/a
9	CHD1	chr14:105262284-105262391	GM12878	blood:	n/a	n/a
10	CHD2	chr14:105261016-105261458	GM12878	blood:	n/a	n/a
11	CHD2	chr14:105262067-105262253	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr14:105262235-105262645	GM12878	blood:	n/a	n/a
13	CHD2	chr14:105262648-105263144	K562	blood:	n/a	n/a
14	CREB1	chr14:105261978-105262243	A549	lung:	n/a	n/a
15	CTCF	chr14:105262620-105262770	GM12866	blood:	n/a	n/a
16	E2F4	chr14:105262245-105262278	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F6	chr14:105261934-105262313	K562	blood:	n/a	chr14:105261969-105261979
18	E2F6	chr14:105262089-105262230	K562	blood:	n/a	n/a
19	EGR1	chr14:105262016-105262562	K562	blood:	n/a	chr14:105262437-105262446 chr14:105262486-105262496 chr14:105262484-105262497 chr14:105262434-105262447 chr14:105262487-105262497 chr14:105262141-105262155
20	EGR1	chr14:105262010-105262261	GM12878	blood:	n/a	chr14:105262141-105262155
21	EGR1	chr14:105262063-105262246	GM12878	blood:	n/a	chr14:105262141-105262155
22	EGR1	chr14:105262068-105262635	K562	blood:	n/a	chr14:105262437-105262446 chr14:105262486-105262496 chr14:105262484-105262497 chr14:105262434-105262447 chr14:105262487-105262497 chr14:105262141-105262155
23	ELF1	chr14:105260962-105261849	GM12878	blood:	n/a	chr14:105261271-105261284 chr14:105261612-105261624 chr14:105261464-105261476 chr14:105261519-105261528 chr14:105261688-105261701
24	ELF1	chr14:105261546-105261789	HepG2	liver:	n/a	chr14:105261612-105261624 chr14:105261688-105261701
25	ELF1	chr14:105261022-105261868	GM12878	blood:	n/a	chr14:105261271-105261284 chr14:105261612-105261624 chr14:105261464-105261476 chr14:105261519-105261528 chr14:105261688-105261701
26	ELF1	chr14:105261469-105261892	K562	blood:	n/a	chr14:105261612-105261624 chr14:105261519-105261528 chr14:105261688-105261701
27	ELF1	chr14:105261429-105261907	K562	blood:	n/a	chr14:105261612-105261624 chr14:105261464-105261476 chr14:105261519-105261528 chr14:105261688-105261701
28	ELK1	chr14:105262343-105262482	GM12878	blood:	n/a	n/a
29	ETS1	chr14:105262123-105262331	K562	blood:	n/a	n/a
30	FOXP2	chr14:105261935-105262429	PFSK-1	brain:	n/a	n/a
31	GABPA	chr14:105261142-105261464	A549	lung:	n/a	n/a
32	GABPA	chr14:105261992-105262250	HepG2	liver:	n/a	n/a
33	GABPA	chr14:105261324-105261733	H1-hESC	embryonic stem cell:	n/a	n/a
34	GABPA	chr14:105261054-105261741	SK-N-SH	brain:	n/a	n/a
35	HA-E2F1	chr14:105261486-105262384	Hela-S3	cervix:	n/a	chr14:105261969-105261979 chr14:105261557-105261566
36	HCFC1	chr14:105262635-105262728	K562	blood:	n/a	n/a
37	HDAC2	chr14:105262657-105263032	HepG2	liver:	n/a	n/a
38	HEY1	chr14:105261917-105262397	K562	blood:	n/a	n/a
39	HEY1	chr14:105261925-105262075	HepG2	liver:	n/a	n/a
40	HEY1	chr14:105261890-105262456	HepG2	liver:	n/a	chr14:105262423-105262438
41	HEY1	chr14:105262553-105263125	HepG2	liver:	n/a	n/a
42	HEY1	chr14:105262552-105262817	HepG2	liver:	n/a	n/a
43	HEY1	chr14:105262140-105262324	HepG2	liver:	n/a	n/a
44	HEY1	chr14:105262122-105262383	K562	blood:	n/a	n/a
45	HMGN3	chr14:105262053-105262541	K562	blood:	n/a	n/a
46	HMGN3	chr14:105261418-105261838	K562	blood:	n/a	n/a
47	HNF4A	chr14:105262616-105263059	HepG2	liver:	n/a	chr14:105262825-105262840 chr14:105262825-105262840 chr14:105262825-105262840 chr14:105262825-105262839
48	HNF4A	chr14:105262610-105262958	HepG2	liver:	n/a	chr14:105262825-105262840 chr14:105262825-105262840 chr14:105262825-105262840 chr14:105262825-105262839
49	HNF4G	chr14:105262675-105263009	HepG2	liver:	n/a	chr14:105262825-105262840 chr14:105262823-105262838 chr14:105262825-105262840 chr14:105262825-105262840 chr14:105262825-105262839
50	JUND	chr14:105261830-105262378	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105262348-105262398	SK-N-SH_RA	brain:	n/a
2	chr14:105262348-105262398	SK-N-SH_RA	brain:	n/a
3	chr14:105262269-105262319	RPTEC	kidney:	n/a
4	chr14:105262269-105262319	HL-60	blood:	n/a
5	chr14:105262305-105262355	AG09319	gingival:	n/a
6	chr14:105262406-105262456	U87	brain:	n/a
7	chr14:105262269-105262319	ECC-1	luminal epithelium:	n/a
8	chr14:105261564-105261614	HL-60	blood:	n/a
9	chr14:105261564-105261614	HMEC	breast:	n/a
10	chr14:105262406-105262456	HL-60	blood:	n/a
11	chr14:105262305-105262355	Hepatocyte	liver:	n/a
12	chr14:105262348-105262398	NHDF-neo	bronchial:	n/a
13	chr14:105261564-105261614	NT2-D1	testis:	n/a
14	chr14:105262348-105262398	HNPCEpiC	eye:	n/a
15	chr14:105262348-105262398	HAEpiC	amniotic membrane:	n/a
16	chr14:105262406-105262456	BJ	skin:	n/a
17	chr14:105262269-105262319	BE2_C	brain:	n/a
18	chr14:105262276-105262326	HMEC	breast:	n/a
19	chr14:105262276-105262326	BE2_C	brain:	n/a
20	chr14:105262348-105262398	HCT-116	colon:	n/a
21	chr14:105262348-105262398	ECC-1	luminal epithelium:	n/a
22	chr14:105262305-105262355	AoSMC	blood vessel:	n/a
23	chr14:105262276-105262326	SAEC	small airway:	n/a
24	chr14:105262276-105262326	MCF-7	breast:	n/a
25	chr14:105262269-105262319	Jurkat	blood:	n/a
26	chr14:105262305-105262355	HEK293	kidney:	embryo
27	chr14:105262348-105262398	HUVEC	blood vessel:	n/a
28	chr14:105261564-105261614	PrEC	prostate:	n/a
29	chr14:105262406-105262456	PANC-1	pancreas:	n/a
30	chr14:105262276-105262326	HCM	heart:	n/a
31	chr14:105262348-105262398	HIPEpiC	eye:	n/a
32	chr14:105262348-105262398	HepG2	liver:	n/a
33	chr14:105262305-105262355	HL-60	blood:	n/a
34	chr14:105262305-105262355	GM19239	blood:	n/a
35	chr14:105262348-105262398	NB4	blood:	n/a
36	chr14:105261564-105261614	LNCaP	prostate:	n/a
37	chr14:105261564-105261614	Hepatocyte	liver:	n/a
38	chr14:105262276-105262326	HIPEpiC	eye:	n/a
39	chr14:105262276-105262326	SK-N-SH	brain:	n/a
40	chr14:105262348-105262398	A549	lung:	n/a
41	chr14:105262305-105262355	CMK	blood:	n/a
42	chr14:105262406-105262456	AG04449	skin:	fetal
43	chr14:105262269-105262319	AG10803	skin:	n/a
44	chr14:105261564-105261614	HEEpiC	esophagus:	n/a
45	chr14:105262406-105262456	HAEpiC	amniotic membrane:	n/a
46	chr14:105262348-105262398	AG04450	lung:	fetal
47	chr14:105261564-105261614	H1-hESC	embryonic stem cell:	embryo
48	chr14:105262269-105262319	PrEC	prostate:	n/a
49	chr14:105262406-105262456	SKMC	muscle:	n/a
50	chr14:105261564-105261614	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105145208..105149817-chr14:105259856..105263393,4	MCF-7	breast:
2	chr14:105190071..105193724-chr14:105262102..105266779,4	K562	blood:
3	chr14:105260251..105263637-chr14:105331262..105334523,4	K562	blood:
4	chr14:105189251..105191715-chr14:105260176..105263336,3	MCF-7	breast:
5	chr14:105261442..105265036-chr14:105329931..105332556,6	MCF-7	breast:
6	chr10:102825608..102826586-chr14:105261508..105262019,2	Hela-S3	cervix:
7	chr14:105234268..105237912-chr14:105260331..105262677,3	K562	blood:
8	chr14:105219293..105222032-chr14:105260458..105263797,3	MCF-7	breast:
9	chr14:105188879..105190553-chr14:105260910..105263562,2	MCF-7	breast:
10	chr14:105259095..105269353-chr14:105280422..105289302,26	K562	blood:
11	chr14:105260375..105263562-chr14:105329763..105332955,5	MCF-7	breast:
12	chr1:153643198..153643841-chr14:105262172..105262866,2	Hela-S3	cervix:

Variant related genes	Relation type
ZBTB42	TF binding region
AKT1	TF binding region
ZBTB42	CpG island
AKT1	CpG island
ENSG00000256050	chromatin interactions
ENSG00000107821	chromatin interactions
ENSG00000143621	chromatin interactions
ENSG00000185100	chromatin interactions
ENSG00000258701	chromatin interactions
ENSG00000258430	chromatin interactions
ENSG00000099814	chromatin interactions
ENSG00000184990	chromatin interactions

Extended variants
information (count: 16 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558659108	chr14:105261529-105261530	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs200512697	chr14:105262025-105262026	Weak transcription Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs575429386	chr14:105262041-105262042	Weak transcription Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs3002448	chr14:105262042-105262043	Weak transcription Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs192433222	chr14:105262309-105262310	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs376844098	chr14:105262350-105262351	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs534197838	chr14:105262360-105262361	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs2498786	chr14:105262368-105262369	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs543348675	chr14:105262441-105262442	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs559806193	chr14:105262446-105262447	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs183769910	chr14:105262476-105262477	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs551571963	chr14:105262591-105262592	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs530000363	chr14:105262624-105262625	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs71129248	chr14:105262664-105262665	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs565020326	chr14:105262691-105262692	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs530937526	chr14:105262701-105262702	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105260200-105261600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:105260200-105262600	Active TSS	H9 Cell Line	embryonic stem cell
3	chr14:105260400-105261600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
4	chr14:105260400-105261600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
5	chr14:105260400-105261800	Flanking Active TSS	Primary hematopoietic stem cells	blood
6	chr14:105260400-105261800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
7	chr14:105260400-105262200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr14:105260400-105262400	Active TSS	HSMMtube	muscle
9	chr14:105260400-105262600	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr14:105260600-105261600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr14:105260600-105261600	Active TSS	Placenta Amnion	Placenta Amnion
12	chr14:105260600-105262200	Active TSS	NHLF	lung
13	chr14:105260600-105262400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:105260600-105262600	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr14:105260600-105262600	Active TSS	HSMM	muscle
16	chr14:105260800-105261600	Flanking Active TSS	Primary B cells from cord blood	blood
17	chr14:105260800-105261600	Active TSS	NHDF-Ad	bronchial
18	chr14:105260800-105261800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:105260800-105262200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:105260800-105262200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr14:105260800-105262200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr14:105260800-105262200	Active TSS	Sigmoid Colon	Sigmoid Colon
23	chr14:105260800-105262400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr14:105260800-105262400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr14:105260800-105262400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr14:105260800-105262400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr14:105260800-105262400	Active TSS	Gastric	stomach
28	chr14:105260800-105262400	Active TSS	Right Atrium	heart
29	chr14:105260800-105262400	Active TSS	Small Intestine	intestine
30	chr14:105260800-105262400	Active TSS	A549	lung
31	chr14:105260800-105262600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr14:105260800-105262600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr14:105261000-105262200	Active TSS	Muscle Satellite Cultured Cells	--
34	chr14:105261000-105262200	Active TSS	Rectal Smooth Muscle	rectum
35	chr14:105261000-105262200	Active TSS	HMEC	breast
36	chr14:105261000-105262200	Active TSS	HUVEC	blood vessel
37	chr14:105261000-105262400	Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr14:105261000-105262400	Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr14:105261000-105262400	Active TSS	HUES64 Cell Line	embryonic stem cell
40	chr14:105261000-105262400	Active TSS	Breast Myoepithelial Primary Cells	Breast
41	chr14:105261000-105262400	Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr14:105261000-105262400	Active TSS	Fetal Intestine Small	intestine
43	chr14:105261000-105262400	Active TSS	GM12878-XiMat	blood
44	chr14:105261000-105262400	Active TSS	Osteobl	bone
45	chr14:105261000-105262600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr14:105261000-105262600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
47	chr14:105261000-105262600	Active TSS	NHEK	skin
48	chr14:105261000-105262800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr14:105261200-105261600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
50	chr14:105261200-105261600	Active TSS	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links