Variant report

Variant	esv1847064
Chromosome Location	chr13:96740247-96743232
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:46)
CpG islands
(count:550)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:46 , 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	chr13:96742943-96744222	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTBP2	chr13:96742083-96742625	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr13:96742337-96742406	MCF-7	breast:	n/a	n/a
5	E2F4	chr13:96741744-96741879	MCF10A-Er-Src	breast:	n/a	n/a
6	E2F6	chr13:96742909-96743319	H1-hESC	embryonic stem cell:	n/a	chr13:96742928-96742938
7	E2F6	chr13:96742190-96742904	H1-hESC	embryonic stem cell:	n/a	chr13:96742303-96742310 chr13:96742302-96742310
8	FOXA1	chr13:96742188-96742499	T-47D	breast:	n/a	n/a
9	HMGN3	chr13:96742924-96743060	K562	blood:	n/a	n/a
10	KAP1	chr13:96741744-96742420	HEK293	kidney:	n/a	n/a
11	MAX	chr13:96742155-96742599	MCF-7	breast:	n/a	n/a
12	MAX	chr13:96742123-96742917	H1-hESC	embryonic stem cell:	n/a	n/a
13	MAX	chr13:96742094-96743289	H1-hESC	embryonic stem cell:	n/a	n/a
14	MAX	chr13:96742124-96742661	ECC-1	luminal epithelium:	n/a	n/a
15	MAX	chr13:96742133-96742806	ECC-1	luminal epithelium:	n/a	n/a
16	MXI1	chr13:96741506-96741539	H1-hESC	embryonic stem cell:	n/a	n/a
17	MXI1	chr13:96742242-96742520	H1-hESC	embryonic stem cell:	n/a	n/a
18	MYC	chr13:96742339-96742398	MCF-7	breast:	n/a	n/a
19	MYC	chr13:96743119-96743195	MCF-7	breast:	n/a	n/a
20	MYC	chr13:96742325-96742362	MCF-7	breast:	n/a	n/a
21	MYC	chr13:96742399-96742415	MCF-7	breast:	n/a	n/a
22	MYC	chr13:96742315-96742365	H1-hESC	embryonic stem cell:	n/a	n/a
23	MYC	chr13:96742308-96742531	MCF-7	breast:	n/a	n/a
24	NFIC	chr13:96742138-96742624	ECC-1	luminal epithelium:	n/a	chr13:96742179-96742196
25	POLR2A	chr13:96740376-96740402	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr13:96741354-96741405	Gliobla	brain:	n/a	n/a
27	POLR2A	chr13:96742047-96742707	MCF-7	breast:	n/a	n/a
28	POLR2A	chr13:96741910-96742583	H1-neurons	neurons:	n/a	n/a
29	POLR2A	chr13:96742050-96742667	MCF-7	breast:	n/a	n/a
30	POLR2A	chr13:96742332-96742493	Gliobla	brain:	n/a	n/a
31	POLR2A	chr13:96742144-96742623	HEK293	kidney:	n/a	n/a
32	POLR2A	chr13:96742117-96742568	H1-neurons	neurons:	n/a	n/a
33	POLR2A	chr13:96742201-96742553	ECC-1	luminal epithelium:	n/a	n/a
34	POLR2A	chr13:96742031-96744213	MCF-7	breast:	n/a	n/a
35	POLR2A	chr13:96742192-96742592	ECC-1	luminal epithelium:	n/a	n/a
36	POLR2A	chr13:96742147-96742444	ProgFib	skin:	n/a	n/a
37	RAD21	chr13:96741992-96742438	H1-hESC	embryonic stem cell:	n/a	n/a
38	SIN3A	chr13:96742048-96743208	H1-hESC	embryonic stem cell:	n/a	chr13:96742718-96742729
39	TAF1	chr13:96742216-96742480	H1-hESC	embryonic stem cell:	n/a	n/a
40	TBP	chr13:96742108-96742559	H1-hESC	embryonic stem cell:	n/a	n/a
41	TBP	chr13:96742925-96743032	H1-hESC	embryonic stem cell:	n/a	n/a
42	UBTF	chr13:96742459-96742469	K562	blood:	n/a	n/a
43	UBTF	chr13:96742704-96742852	K562	blood:	n/a	n/a
44	WRNIP1	chr13:96741985-96742029	GM12878	blood:	n/a	n/a
45	ZNF143	chr13:96742084-96742597	H1-hESC	embryonic stem cell:	n/a	n/a
46	ZNF263	chr13:96741220-96743141	HEK293-T-REx	kidney:	n/a	chr13:96742265-96742274 chr13:96742224-96742245

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96742056-96742106	U87	brain:	n/a
2	chr13:96742056-96742106	U87	brain:	n/a
3	chr13:96742905-96742955	HRE	kidney:	n/a
4	chr13:96742413-96742463	SK-N-SH_RA	brain:	n/a
5	chr13:96743110-96743160	H1-hESC	embryonic stem cell:	embryo
6	chr13:96742421-96742471	A549	lung:	n/a
7	chr13:96741314-96741364	Hepatocyte	liver:	n/a
8	chr13:96743110-96743160	HUVEC	blood vessel:	n/a
9	chr13:96742905-96742955	AG09309	skin:	n/a
10	chr13:96743110-96743160	ProgFib	skin:	n/a
11	chr13:96742421-96742471	PrEC	prostate:	n/a
12	chr13:96742413-96742463	SKMC	muscle:	n/a
13	chr13:96743110-96743160	HEK293	kidney:	embryo
14	chr13:96741314-96741364	HCF	heart:	n/a
15	chr13:96743110-96743160	Caco-2	colon:	n/a
16	chr13:96743110-96743160	MCF-7	breast:	n/a
17	chr13:96742905-96742955	ProgFib	skin:	n/a
18	chr13:96743110-96743160	T-47D	breast:	n/a
19	chr13:96742056-96742106	PANC-1	pancreas:	n/a
20	chr13:96742413-96742463	HAEpiC	amniotic membrane:	n/a
21	chr13:96741314-96741364	MCF-7	breast:	n/a
22	chr13:96743087-96743137	SK-N-MC	brain:	n/a
23	chr13:96742905-96742955	AG04450	lung:	fetal
24	chr13:96742421-96742471	RPTEC	kidney:	n/a
25	chr13:96742905-96742955	BJ	skin:	n/a
26	chr13:96742317-96742367	GM12878	blood:	n/a
27	chr13:96743170-96743220	AoSMC	blood vessel:	n/a
28	chr13:96742317-96742367	HIPEpiC	eye:	n/a
29	chr13:96742413-96742463	AG10803	skin:	n/a
30	chr13:96742056-96742106	AG09309	skin:	n/a
31	chr13:96743087-96743137	IMR90	lung:	fetal
32	chr13:96742905-96742955	ovcar-3	ovarian:	n/a
33	chr13:96742413-96742463	HEEpiC	esophagus:	n/a
34	chr13:96743170-96743220	MCF10A-Er-Src	breast:	n/a
35	chr13:96741314-96741364	NHBE	bronchial:	n/a
36	chr13:96741314-96741364	NT2-D1	testis:	n/a
37	chr13:96743170-96743220	ECC-1	luminal epithelium:	n/a
38	chr13:96742056-96742106	T-47D	breast:	n/a
39	chr13:96742056-96742106	AG09319	gingival:	n/a
40	chr13:96741314-96741364	LNCaP	prostate:	n/a
41	chr13:96742317-96742367	GM06990	blood:	n/a
42	chr13:96742317-96742367	SK-N-SH_RA	brain:	n/a
43	chr13:96743087-96743137	HAEpiC	amniotic membrane:	n/a
44	chr13:96742056-96742106	NT2-D1	testis:	n/a
45	chr13:96743087-96743137	GM12878	blood:	n/a
46	chr13:96743087-96743137	HRPEpiC	eye:	n/a
47	chr13:96743087-96743137	Hepatocyte	liver:	n/a
48	chr13:96742317-96742367	HEEpiC	esophagus:	n/a
49	chr13:96742056-96742106	HCF	heart:	n/a
50	chr13:96742421-96742471	AG10803	skin:	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: 86 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:86 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs593806	chr13:96740247-96740248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs193290659	chr13:96740252-96740253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111584207	chr13:96740271-96740272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34934639	chr13:96740278-96740279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs71434511	chr13:96740310-96740311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139808821	chr13:96740315-96740316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184999479	chr13:96740390-96740391	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs199624294	chr13:96740423-96740424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188756393	chr13:96740430-96740431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143710686	chr13:96740482-96740483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146807406	chr13:96740489-96740490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558695843	chr13:96740569-96740570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575365380	chr13:96740584-96740585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139522900	chr13:96740672-96740673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192594040	chr13:96740719-96740720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183937607	chr13:96740732-96740733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374388259	chr13:96740737-96740738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576414190	chr13:96740817-96740818	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367562618	chr13:96740819-96740820	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560126881	chr13:96740898-96740899	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372104945	chr13:96740931-96740932	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576634535	chr13:96741102-96741103	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs481049	chr13:96741182-96741183	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs577470309	chr13:96741226-96741227	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs530877416	chr13:96741233-96741234	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs367959458	chr13:96741237-96741238	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs188664851	chr13:96741328-96741329	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550732379	chr13:96741341-96741342	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs180829755	chr13:96741360-96741361	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs34763066	chr13:96741365-96741366	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs530373161	chr13:96741395-96741396	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs547263882	chr13:96741408-96741409	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs59409680	chr13:96741415-96741416	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs75538526	chr13:96741468-96741469	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs144181915	chr13:96741469-96741470	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs145431571	chr13:96741513-96741514	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs183767516	chr13:96741554-96741555	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs531284980	chr13:96741613-96741614	Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs4547219	chr13:96741656-96741657	Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs11616724	chr13:96741670-96741671	Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs34481001	chr13:96741683-96741684	Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs533511056	chr13:96741713-96741714	Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs190225954	chr13:96741778-96741779	Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs182409868	chr13:96741804-96741805	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
45	rs576695840	chr13:96741852-96741853	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
46	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
47	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
48	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
49	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
50	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

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:229 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96734800-96740800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr13:96740800-96741000	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr13:96740800-96741200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:96741000-96741400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr13:96741200-96741800	Enhancers	Pancreas	Pancrea
6	chr13:96741400-96741600	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr13:96741600-96741800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr13:96741600-96742400	Bivalent/Poised TSS	Fetal Kidney	kidney
9	chr13:96741600-96742600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr13:96741600-96744200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
11	chr13:96741800-96742000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr13:96741800-96742000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
13	chr13:96741800-96742000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
14	chr13:96741800-96742000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
15	chr13:96741800-96742000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr13:96741800-96742000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr13:96741800-96742000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr13:96741800-96742000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
19	chr13:96741800-96742000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr13:96741800-96742000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr13:96741800-96742000	Bivalent/Poised TSS	Adipose Nuclei	Adipose
22	chr13:96741800-96742000	Bivalent Enhancer	Liver	Liver
23	chr13:96741800-96742000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
24	chr13:96741800-96742000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
25	chr13:96741800-96742000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
26	chr13:96741800-96742000	Flanking Bivalent TSS/Enh	Fetal Heart	heart
27	chr13:96741800-96742000	Bivalent Enhancer	Fetal Intestine Small	intestine
28	chr13:96741800-96742000	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
29	chr13:96741800-96742000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
30	chr13:96741800-96742000	Bivalent Enhancer	HepG2	liver
31	chr13:96741800-96742200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
32	chr13:96741800-96742200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
33	chr13:96741800-96742200	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
34	chr13:96741800-96742200	Bivalent Enhancer	Fetal Brain Male	brain
35	chr13:96741800-96742200	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
36	chr13:96741800-96742400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr13:96741800-96742400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
38	chr13:96741800-96742400	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
39	chr13:96741800-96742400	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
40	chr13:96741800-96742600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
41	chr13:96741800-96742600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr13:96741800-96742600	Flanking Active TSS	Pancreas	Pancrea
43	chr13:96741800-96742600	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
44	chr13:96741800-96743200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr13:96741800-96743400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
46	chr13:96741800-96743400	Bivalent/Poised TSS	Right Ventricle	heart
47	chr13:96741800-96743600	Active TSS	Brain Substantia Nigra	brain
48	chr13:96741800-96744000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr13:96741800-96744400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
50	chr13:96741800-96744400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell

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