Variant report

Variant	esv13446
Chromosome Location	chr6:15248316-15249040
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	chr6:15248898-15249053	K562	blood:	n/a	n/a
2	ARID3A	chr6:15248850-15249511	HepG2	liver:	n/a	n/a
3	ATF1	chr6:15248767-15249548	K562	blood:	n/a	chr6:15248837-15248851
4	ATF2	chr6:15248700-15249611	GM12878	blood:	n/a	chr6:15248837-15248851
5	ATF2	chr6:15248758-15249043	H1-hESC	embryonic stem cell:	n/a	chr6:15248837-15248851
6	ATF2	chr6:15248766-15249202	H1-hESC	embryonic stem cell:	n/a	chr6:15248837-15248851
7	ATF2	chr6:15248786-15249160	GM12878	blood:	n/a	chr6:15248837-15248851
8	ATF2	chr6:15248031-15248469	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr6:15248775-15249024	K562	blood:	n/a	chr6:15248975-15248982 chr6:15248971-15248986 chr6:15248974-15248982 chr6:15248975-15248983 chr6:15248973-15248984
10	BACH1	chr6:15248886-15249269	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr6:15248661-15249053	GM12878	blood:	n/a	chr6:15248721-15248734
12	BCLAF1	chr6:15248816-15249721	GM12878	blood:	n/a	chr6:15249305-15249314
13	BCLAF1	chr6:15248714-15249801	GM12878	blood:	n/a	chr6:15248721-15248734 chr6:15249305-15249314
14	BHLHE40	chr6:15248777-15249312	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:15248091-15248489	K562	blood:	n/a	n/a
16	BHLHE40	chr6:15248730-15249435	K562	blood:	n/a	n/a
17	BRCA1	chr6:15248874-15249298	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr6:15248838-15249083	GM12878	blood:	n/a	n/a
19	BRCA1	chr6:15248771-15249972	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr6:15248850-15249143	HepG2	liver:	n/a	n/a
21	CBX3	chr6:15248648-15249734	K562	blood:	n/a	n/a
22	CCNT2	chr6:15247939-15249553	K562	blood:	n/a	n/a
23	CEBPB	chr6:15248784-15250234	Hela-S3	cervix:	n/a	chr6:15250010-15250019 chr6:15250010-15250019 chr6:15250008-15250019
24	CEBPB	chr6:15248902-15249526	HepG2	liver:	n/a	n/a
25	CEBPD	chr6:15248626-15249436	K562	blood:	n/a	n/a
26	CEBPD	chr6:15248661-15249274	K562	blood:	n/a	n/a
27	CEBPD	chr6:15248668-15249399	HepG2	liver:	n/a	n/a
28	CHD1	chr6:15248042-15248427	GM12878	blood:	n/a	n/a
29	CHD1	chr6:15246112-15248421	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr6:15244739-15251552	IMR90	lung:	n/a	chr6:15245627-15245637 chr6:15245113-15245123
31	CHD2	chr6:15247900-15249524	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr6:15248776-15249553	GM12878	blood:	n/a	n/a
33	CHD2	chr6:15248866-15249329	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr6:15248784-15249308	HepG2	liver:	n/a	n/a
35	CHD2	chr6:15248304-15248490	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr6:15248685-15249521	K562	blood:	n/a	n/a
37	CHD2	chr6:15248204-15248449	HepG2	liver:	n/a	n/a
38	CREB1	chr6:15247845-15250008	K562	blood:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
39	CREB1	chr6:15248659-15249726	GM12878	blood:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
40	CREB1	chr6:15248643-15249516	H1-hESC	embryonic stem cell:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
41	CREB1	chr6:15247870-15249858	GM12878	blood:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
42	CREB1	chr6:15248700-15249173	A549	lung:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
43	CREB1	chr6:15248155-15249672	HepG2	liver:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
44	CREB1	chr6:15248632-15249953	K562	blood:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
45	CREB1	chr6:15248012-15249697	HepG2	liver:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
46	CREB1	chr6:15248096-15249493	A549	lung:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
47	CREB1	chr6:15248715-15249259	ECC-1	luminal epithelium:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
48	CREB1	chr6:15248651-15249485	H1-hESC	embryonic stem cell:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
49	CREB1	chr6:15248713-15249263	ECC-1	luminal epithelium:	n/a	chr6:15248972-15248985 chr6:15249021-15249034
50	CTCF	chr6:15248483-15248573	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:15248611-15248661	PANC-1	pancreas:	n/a
2	chr6:15248932-15248982	SK-N-MC	brain:	n/a
3	chr6:15248335-15248385	GM12878	blood:	n/a
4	chr6:15248936-15248986	AG10803	skin:	n/a
5	chr6:15248932-15248982	HNPCEpiC	eye:	n/a
6	chr6:15248611-15248661	ECC-1	luminal epithelium:	n/a
7	chr6:15248932-15248982	SK-N-SH	brain:	n/a
8	chr6:15248936-15248986	Caco-2	colon:	n/a
9	chr6:15248611-15248661	NT2-D1	testis:	n/a
10	chr6:15248611-15248661	NB4	blood:	n/a
11	chr6:15248932-15248982	AG09309	skin:	n/a
12	chr6:15248335-15248385	AoSMC	blood vessel:	n/a
13	chr6:15248611-15248661	GM12891	blood:	n/a
14	chr6:15248611-15248661	SKMC	muscle:	n/a
15	chr6:15248335-15248385	NHBE	bronchial:	n/a
16	chr6:15248936-15248986	AG09319	gingival:	n/a
17	chr6:15248335-15248385	AG09309	skin:	n/a
18	chr6:15248611-15248661	HMEC	breast:	n/a
19	chr6:15248936-15248986	HMEC	breast:	n/a
20	chr6:15248335-15248385	GM06990	blood:	n/a
21	chr6:15248932-15248982	GM06990	blood:	n/a
22	chr6:15248932-15248982	Hepatocyte	liver:	n/a
23	chr6:15248611-15248661	NHDF-neo	bronchial:	n/a
24	chr6:15248611-15248661	HIPEpiC	eye:	n/a
25	chr6:15248335-15248385	ProgFib	skin:	n/a
26	chr6:15248936-15248986	CMK	blood:	n/a
27	chr6:15248335-15248385	T-47D	breast:	n/a
28	chr6:15248932-15248982	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:15248611-15248661	HAEpiC	amniotic membrane:	n/a
30	chr6:15248936-15248986	HCF	heart:	n/a
31	chr6:15248335-15248385	RPTEC	kidney:	n/a
32	chr6:15248936-15248986	Hela-S3	cervix:	n/a
33	chr6:15248611-15248661	AG04449	skin:	fetal
34	chr6:15248932-15248982	SAEC	small airway:	n/a
35	chr6:15248335-15248385	AG04450	lung:	fetal
36	chr6:15248611-15248661	HEEpiC	esophagus:	n/a
37	chr6:15248936-15248986	SAEC	small airway:	n/a
38	chr6:15248611-15248661	MCF-7	breast:	n/a
39	chr6:15248335-15248385	HNPCEpiC	eye:	n/a
40	chr6:15248335-15248385	BE2_C	brain:	n/a
41	chr6:15248611-15248661	HepG2	liver:	n/a
42	chr6:15248335-15248385	Hela-S3	cervix:	n/a
43	chr6:15248611-15248661	SAEC	small airway:	n/a
44	chr6:15248936-15248986	HRCEpiC	kidney:	n/a
45	chr6:15248335-15248385	NT2-D1	testis:	n/a
46	chr6:15248335-15248385	HRPEpiC	eye:	n/a
47	chr6:15248936-15248986	Jurkat	blood:	n/a
48	chr6:15248611-15248661	HRCEpiC	kidney:	n/a
49	chr6:15248611-15248661	U87	brain:	n/a
50	chr6:15248611-15248661	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:15247857..15248661-chr6:15441250..15442133,2	MCF-7	breast:
2	chr18:57566476..57568620-chr6:15247479..15249980,2	K562	blood:
3	chr6:14695043..14697656-chr6:15246930..15248844,2	K562	blood:
4	chr6:15248895..15250425-chr6:16129384..16130957,2	K562	blood:
5	chr6:15147856..15151805-chr6:15244004..15248641,4	MCF-7	breast:
6	chr6:15088518..15090840-chr6:15243708..15248817,8	MCF-7	breast:
7	chr6:15087697..15092455-chr6:15243972..15249952,11	K562	blood:
8	chr1:155278025..155278903-chr6:15248328..15249078,2	Hela-S3	cervix:
9	chr6:15248004..15250330-chr6:15324617..15327935,3	K562	blood:
10	chr6:15090854..15092609-chr6:15247191..15248815,2	MCF-7	breast:
11	chr6:15085986..15094450-chr6:15243173..15249347,32	MCF-7	breast:
12	chr6:15248659..15249502-chr6:18155621..18156172,2	Hela-S3	cervix:
13	chr6:15247440..15249791-chr6:15324617..15327427,3	K562	blood:
14	chr6:15087836..15090279-chr6:15247303..15249952,4	K562	blood:
15	chr12:54673793..54674774-chr6:15248174..15248787,2	Hela-S3	cervix:
16	chr6:15238350..15240596-chr6:15246578..15248795,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTNBP1-3	chr6:15248741-15248887	NONHSAT107868
2	lnc-DTNBP1-3	chr6:15248049-15248375	NONHSAT107868

Variant related genes	Relation type
JARID2-AS1	TF binding region
JARID2	TF binding region
ENSG00000271888	TF binding region
JARID2-AS1	CpG island
JARID2	CpG island
ENSG00000271888	CpG island
ENSG00000007944	chromatin interactions
ENSG00000264687	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000165097	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000201519	chromatin interactions
ENSG00000234261	chromatin interactions
ENSG00000141682	chromatin interactions
ENSG00000135486	chromatin interactions

Extended variants
information (count: 16 )
Associated
traits (count: 101 )

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	rs563992240	chr6:15248323-15248324	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
2	rs149370723	chr6:15248332-15248333	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
3	rs552116785	chr6:15248335-15248336	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
4	rs565856769	chr6:15248340-15248341	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
5	rs534787498	chr6:15248345-15248346	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
6	rs559825178	chr6:15248358-15248359	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
7	rs111928694	chr6:15248364-15248365	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
8	rs548799494	chr6:15248388-15248389	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs576495888	chr6:15248389-15248390	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs563406132	chr6:15248493-15248494	Weak transcription Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs566059888	chr6:15248501-15248502	Weak transcription Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs113213471	chr6:15248568-15248569	Weak transcription Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs529269902	chr6:15248780-15248781	Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
14	rs577575434	chr6:15248909-15248910	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs144135052	chr6:15248947-15248948	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs548926032	chr6:15249036-15249037	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Cancer	16790693	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15243200-15248400	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr6:15243600-15250200	Active TSS	H9 Cell Line	embryonic stem cell
3	chr6:15243800-15248400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr6:15244000-15250000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:15244200-15249400	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr6:15244200-15249800	Active TSS	Rectal Smooth Muscle	rectum
7	chr6:15244400-15249200	Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr6:15244400-15249400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr6:15244400-15249600	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr6:15244400-15250200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr6:15244400-15250400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:15244600-15248400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:15244600-15248400	Active TSS	NHDF-Ad	bronchial
14	chr6:15244600-15249200	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr6:15244600-15249200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:15244600-15249200	Active TSS	Duodenum Mucosa	Duodenum
17	chr6:15244600-15249200	Active TSS	NH-A	brain
18	chr6:15244600-15249200	Active TSS	Osteobl	bone
19	chr6:15244600-15249400	Active TSS	H1 Cell Line	embryonic stem cell
20	chr6:15244600-15249400	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr6:15244600-15249400	Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr6:15244600-15249400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:15244600-15249400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr6:15244600-15249400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr6:15244600-15249400	Active TSS	Brain Anterior Caudate	brain
26	chr6:15244600-15249400	Active TSS	Fetal Intestine Large	intestine
27	chr6:15244600-15249400	Active TSS	Thymus	Thymus
28	chr6:15244600-15249400	Active TSS	HSMM	muscle
29	chr6:15244600-15249600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:15244600-15249600	Active TSS	Brain Angular Gyrus	brain
31	chr6:15244600-15249600	Active TSS	Right Ventricle	heart
32	chr6:15244600-15249800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
33	chr6:15244600-15249800	Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr6:15244600-15249800	Active TSS	Ovary	ovary
35	chr6:15244600-15249800	Active TSS	Psoas Muscle	Psoas
36	chr6:15244600-15250000	Active TSS	NHLF	lung
37	chr6:15244600-15250200	Active TSS	A549	lung
38	chr6:15244600-15250400	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr6:15244800-15249200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr6:15244800-15249200	Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr6:15244800-15249200	Active TSS	Left Ventricle	heart
42	chr6:15244800-15249200	Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr6:15244800-15249400	Active TSS	Brain Substantia Nigra	brain
44	chr6:15244800-15249400	Active TSS	Fetal Kidney	kidney
45	chr6:15244800-15249400	Active TSS	Fetal Lung	lung
46	chr6:15244800-15249400	Active TSS	Lung	lung
47	chr6:15244800-15249600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr6:15244800-15249600	Active TSS	Gastric	stomach
49	chr6:15244800-15249600	Active TSS	HSMMtube	muscle
50	chr6:15244800-15249800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links