Variant report

Variant	nsv562780
Chromosome Location	chr13:96741862-96742681
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:37)
CpG islands
(count:244)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:37 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD1	chr13:96742349-96742595	H1-hESC	embryonic stem cell:	n/a	chr13:96742482-96742492
2	CTBP2	chr13:96742083-96742625	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr13:96742337-96742406	MCF-7	breast:	n/a	n/a
4	E2F4	chr13:96741744-96741879	MCF10A-Er-Src	breast:	n/a	n/a
5	E2F6	chr13:96742190-96742904	H1-hESC	embryonic stem cell:	n/a	chr13:96742303-96742310 chr13:96742302-96742310
6	FOXA1	chr13:96742188-96742499	T-47D	breast:	n/a	n/a
7	KAP1	chr13:96741744-96742420	HEK293	kidney:	n/a	n/a
8	MAX	chr13:96742123-96742917	H1-hESC	embryonic stem cell:	n/a	n/a
9	MAX	chr13:96742133-96742806	ECC-1	luminal epithelium:	n/a	n/a
10	MAX	chr13:96742155-96742599	MCF-7	breast:	n/a	n/a
11	MAX	chr13:96742124-96742661	ECC-1	luminal epithelium:	n/a	n/a
12	MAX	chr13:96742094-96743289	H1-hESC	embryonic stem cell:	n/a	n/a
13	MXI1	chr13:96742242-96742520	H1-hESC	embryonic stem cell:	n/a	n/a
14	MYC	chr13:96742399-96742415	MCF-7	breast:	n/a	n/a
15	MYC	chr13:96742325-96742362	MCF-7	breast:	n/a	n/a
16	MYC	chr13:96742308-96742531	MCF-7	breast:	n/a	n/a
17	MYC	chr13:96742339-96742398	MCF-7	breast:	n/a	n/a
18	MYC	chr13:96742315-96742365	H1-hESC	embryonic stem cell:	n/a	n/a
19	NFIC	chr13:96742138-96742624	ECC-1	luminal epithelium:	n/a	chr13:96742179-96742196
20	POLR2A	chr13:96742332-96742493	Gliobla	brain:	n/a	n/a
21	POLR2A	chr13:96742117-96742568	H1-neurons	neurons:	n/a	n/a
22	POLR2A	chr13:96742050-96742667	MCF-7	breast:	n/a	n/a
23	POLR2A	chr13:96742031-96744213	MCF-7	breast:	n/a	n/a
24	POLR2A	chr13:96742047-96742707	MCF-7	breast:	n/a	n/a
25	POLR2A	chr13:96742192-96742592	ECC-1	luminal epithelium:	n/a	n/a
26	POLR2A	chr13:96742147-96742444	ProgFib	skin:	n/a	n/a
27	POLR2A	chr13:96742144-96742623	HEK293	kidney:	n/a	n/a
28	POLR2A	chr13:96741910-96742583	H1-neurons	neurons:	n/a	n/a
29	POLR2A	chr13:96742201-96742553	ECC-1	luminal epithelium:	n/a	n/a
30	RAD21	chr13:96741992-96742438	H1-hESC	embryonic stem cell:	n/a	n/a
31	SIN3A	chr13:96742048-96743208	H1-hESC	embryonic stem cell:	n/a	chr13:96742718-96742729
32	TAF1	chr13:96742216-96742480	H1-hESC	embryonic stem cell:	n/a	n/a
33	TBP	chr13:96742108-96742559	H1-hESC	embryonic stem cell:	n/a	n/a
34	UBTF	chr13:96742459-96742469	K562	blood:	n/a	n/a
35	WRNIP1	chr13:96741985-96742029	GM12878	blood:	n/a	n/a
36	ZNF143	chr13:96742084-96742597	H1-hESC	embryonic stem cell:	n/a	n/a
37	ZNF263	chr13:96741220-96743141	HEK293-T-REx	kidney:	n/a	chr13:96742265-96742274 chr13:96742224-96742245

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96742413-96742463	HEEpiC	esophagus:	n/a
2	chr13:96742421-96742471	ovcar-3	ovarian:	n/a
3	chr13:96742413-96742463	Caco-2	colon:	n/a
4	chr13:96742413-96742463	HRE	kidney:	n/a
5	chr13:96742056-96742106	HUVEC	blood vessel:	n/a
6	chr13:96742317-96742367	PrEC	prostate:	n/a
7	chr13:96742317-96742367	HCT-116	colon:	n/a
8	chr13:96742421-96742471	PrEC	prostate:	n/a
9	chr13:96742056-96742106	LNCaP	prostate:	n/a
10	chr13:96742421-96742471	BE2_C	brain:	n/a
11	chr13:96742421-96742471	GM12878	blood:	n/a
12	chr13:96742056-96742106	AG04449	skin:	fetal
13	chr13:96742056-96742106	PrEC	prostate:	n/a
14	chr13:96742421-96742471	PFSK-1	brain:	n/a
15	chr13:96742317-96742367	MCF10A-Er-Src	breast:	n/a
16	chr13:96742413-96742463	LNCaP	prostate:	n/a
17	chr13:96742056-96742106	GM12892	blood:	n/a
18	chr13:96742421-96742471	SK-N-SH_RA	brain:	n/a
19	chr13:96742421-96742471	NHDF-neo	bronchial:	n/a
20	chr13:96742317-96742367	HCF	heart:	n/a
21	chr13:96742413-96742463	Jurkat	blood:	n/a
22	chr13:96742317-96742367	HRPEpiC	eye:	n/a
23	chr13:96742421-96742471	BJ	skin:	n/a
24	chr13:96742421-96742471	HCF	heart:	n/a
25	chr13:96742317-96742367	H1-hESC	embryonic stem cell:	embryo
26	chr13:96742317-96742367	PANC-1	pancreas:	n/a
27	chr13:96742056-96742106	HepG2	liver:	n/a
28	chr13:96742317-96742367	ECC-1	luminal epithelium:	n/a
29	chr13:96742056-96742106	SK-N-SH_RA	brain:	n/a
30	chr13:96742421-96742471	HepG2	liver:	n/a
31	chr13:96742413-96742463	HepG2	liver:	n/a
32	chr13:96742317-96742367	PFSK-1	brain:	n/a
33	chr13:96742317-96742367	HIPEpiC	eye:	n/a
34	chr13:96742413-96742463	HCPEpiC	choroid plexus:	n/a
35	chr13:96742421-96742471	NT2-D1	testis:	n/a
36	chr13:96742413-96742463	SAEC	small airway:	n/a
37	chr13:96742421-96742471	HRPEpiC	eye:	n/a
38	chr13:96742317-96742367	HNPCEpiC	eye:	n/a
39	chr13:96742056-96742106	HEK293	kidney:	embryo
40	chr13:96742056-96742106	NT2-D1	testis:	n/a
41	chr13:96742317-96742367	HL-60	blood:	n/a
42	chr13:96742413-96742463	Hepatocyte	liver:	n/a
43	chr13:96742413-96742463	GM06990	blood:	n/a
44	chr13:96742056-96742106	HL-60	blood:	n/a
45	chr13:96742056-96742106	MCF10A-Er-Src	breast:	n/a
46	chr13:96742421-96742471	HUVEC	blood vessel:	n/a
47	chr13:96742317-96742367	U87	brain:	n/a
48	chr13:96742413-96742463	SKMC	muscle:	n/a
49	chr13:96742056-96742106	HPAEpiC	pulmonary alveolar:	n/a
50	chr13:96742413-96742463	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:96705694..96707387-chr13:96740919..96743720,3	MCF-7	breast:

No data

Variant related genes	Relation type
HS6ST3	TF binding region
HS6ST3	CpG island
ENSG00000102595	chromatin interactions

Extended variants
information (count: 26 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11618108	chr13:96741862-96741863	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149217724	chr13:96741912-96741913	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186636052	chr13:96741940-96741941	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs191938059	chr13:96741941-96741942	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs143356746	chr13:96741951-96741952	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs530116078	chr13:96741977-96741978	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs542092195	chr13:96742014-96742015	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554101300	chr13:96742033-96742034	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs546632514	chr13:96742080-96742081	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576962292	chr13:96742126-96742127	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs532823113	chr13:96742146-96742147	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs151296653	chr13:96742148-96742149	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs569455656	chr13:96742159-96742160	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs74593652	chr13:96742206-96742207	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs548272861	chr13:96742221-96742222	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs72637840	chr13:96742287-96742288	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs533802459	chr13:96742288-96742289	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs553453534	chr13:96742298-96742299	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs140828971	chr13:96742382-96742383	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs150316629	chr13:96742418-96742419	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539325831	chr13:96742425-96742426	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs555987139	chr13:96742441-96742442	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575823438	chr13:96742451-96742452	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs372521314	chr13:96742539-96742540	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs181704452	chr13:96742583-96742584	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs555050103	chr13:96742607-96742608	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96741600-96742400	Bivalent/Poised TSS	Fetal Kidney	kidney
2	chr13:96741600-96742600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr13:96741600-96744200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
4	chr13:96741800-96742000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr13:96741800-96742000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
6	chr13:96741800-96742000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
7	chr13:96741800-96742000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
8	chr13:96741800-96742000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr13:96741800-96742000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr13:96741800-96742000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr13:96741800-96742000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
12	chr13:96741800-96742000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr13:96741800-96742000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr13:96741800-96742000	Bivalent/Poised TSS	Adipose Nuclei	Adipose
15	chr13:96741800-96742000	Bivalent Enhancer	Liver	Liver
16	chr13:96741800-96742000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
17	chr13:96741800-96742000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
18	chr13:96741800-96742000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
19	chr13:96741800-96742000	Flanking Bivalent TSS/Enh	Fetal Heart	heart
20	chr13:96741800-96742000	Bivalent Enhancer	Fetal Intestine Small	intestine
21	chr13:96741800-96742000	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
22	chr13:96741800-96742000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
23	chr13:96741800-96742000	Bivalent Enhancer	HepG2	liver
24	chr13:96741800-96742200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
25	chr13:96741800-96742200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
26	chr13:96741800-96742200	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
27	chr13:96741800-96742200	Bivalent Enhancer	Fetal Brain Male	brain
28	chr13:96741800-96742200	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
29	chr13:96741800-96742400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr13:96741800-96742400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
31	chr13:96741800-96742400	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
32	chr13:96741800-96742400	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
33	chr13:96741800-96742600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
34	chr13:96741800-96742600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr13:96741800-96742600	Flanking Active TSS	Pancreas	Pancrea
36	chr13:96741800-96742600	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
37	chr13:96741800-96743200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr13:96741800-96743400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
39	chr13:96741800-96743400	Bivalent/Poised TSS	Right Ventricle	heart
40	chr13:96741800-96743600	Active TSS	Brain Substantia Nigra	brain
41	chr13:96741800-96744000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr13:96741800-96744400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
43	chr13:96741800-96744400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
44	chr13:96741800-96744400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
45	chr13:96741800-96744600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
46	chr13:96741800-96744600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
47	chr13:96741800-96746000	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr13:96742000-96742200	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr13:96742000-96742200	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr13:96742000-96742200	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived

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