Variant report

Variant	nsv962988
Chromosome Location	chr19:52099340-52106095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:138)
CpG islands
(count:610)
Chromatin interactive
region (count:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:138 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr19:52105602-52106196	GM12878	blood:	n/a	n/a
2	BATF	chr19:52102436-52102722	GM12878	blood:	n/a	n/a
3	BATF	chr19:52105865-52106107	GM12878	blood:	n/a	n/a
4	BCLAF1	chr19:52105617-52106137	GM12878	blood:	n/a	n/a
5	CEBPB	chr19:52098954-52099531	K562	blood:	n/a	chr19:52099245-52099256
6	CEBPB	chr19:52099019-52099403	MCF-7	breast:	n/a	chr19:52099245-52099256
7	CEBPB	chr19:52099075-52099432	IMR90	lung:	n/a	chr19:52099245-52099256
8	CEBPB	chr19:52099030-52099494	K562	blood:	n/a	chr19:52099245-52099256
9	CEBPB	chr19:52099076-52099402	K562	blood:	n/a	chr19:52099245-52099256
10	CEBPB	chr19:52099102-52099364	HepG2	liver:	n/a	chr19:52099245-52099256
11	CEBPB	chr19:52099087-52099419	A549	lung:	n/a	chr19:52099245-52099256
12	CEBPB	chr19:52099145-52099402	Hela-S3	cervix:	n/a	chr19:52099245-52099256
13	CEBPB	chr19:52099074-52099441	HepG2	liver:	n/a	chr19:52099245-52099256
14	CEBPD	chr19:52098975-52099435	K562	blood:	n/a	chr19:52099245-52099256
15	CTCF	chr19:52105840-52105990	GM12871	blood:	n/a	n/a
16	CTCF	chr19:52105900-52106050	GM12872	blood:	n/a	n/a
17	CTCF	chr19:52105880-52106030	GM12875	blood:	n/a	n/a
18	CTCF	chr19:52104453-52104631	GM19238	blood:	n/a	n/a
19	CTCF	chr19:52104665-52104834	GM12878	blood:	n/a	n/a
20	CTCF	chr19:52104440-52104590	GM12865	blood:	n/a	n/a
21	CTCF	chr19:52104460-52104610	GM12864	blood:	n/a	n/a
22	CTCF	chr19:52104467-52104633	GM19239	blood:	n/a	n/a
23	CTCF	chr19:52105800-52105950	GM12875	blood:	n/a	n/a
24	CTCF	chr19:52104520-52104670	GM12864	blood:	n/a	n/a
25	CTCF	chr19:52104763-52104823	GM20000	blood:	n/a	n/a
26	CTCF	chr19:52105880-52106030	GM12869	blood:	n/a	n/a
27	CTCF	chr19:52104440-52104590	GM06990	blood:	n/a	n/a
28	CTCF	chr19:52104695-52104888	GM19239	blood:	n/a	n/a
29	CTCF	chr19:52105820-52105970	GM12878	blood:	n/a	n/a
30	CTCF	chr19:52105740-52105890	GM12868	blood:	n/a	n/a
31	CTCF	chr19:52104493-52104500	GM13976	blood:	n/a	n/a
32	CTCF	chr19:52105476-52105551	GM19239	blood:	n/a	n/a
33	CTCF	chr19:52105640-52105790	GM12865	blood:	n/a	n/a
34	CTCF	chr19:52104690-52104881	GM10266	blood:	n/a	n/a
35	CTCF	chr19:52104540-52104690	GM06990	blood:	n/a	n/a
36	CTCF	chr19:52104704-52104863	GM13976	blood:	n/a	n/a
37	CTCF	chr19:52105880-52106030	GM12871	blood:	n/a	n/a
38	CTCF	chr19:52105860-52106010	GM12864	blood:	n/a	n/a
39	CTCF	chr19:52105740-52105890	GM12878	blood:	n/a	n/a
40	CTCF	chr19:52104580-52104730	GM12865	blood:	n/a	n/a
41	CTCF	chr19:52105800-52105950	GM12873	blood:	n/a	n/a
42	CTCF	chr19:52105880-52106030	GM12865	blood:	n/a	n/a
43	CTCF	chr19:52104400-52104550	GM12870	blood:	n/a	n/a
44	CTCF	chr19:52105866-52106043	GM12878	blood:	n/a	n/a
45	CTCF	chr19:52105944-52106020	GM10248	blood:	n/a	n/a
46	CTCF	chr19:52105939-52106042	GM19238	blood:	n/a	n/a
47	CTCF	chr19:52104600-52104750	GM12866	blood:	n/a	n/a
48	CTCF	chr19:52104600-52104750	GM12867	blood:	n/a	n/a
49	CTCF	chr19:52105920-52106070	GM06990	blood:	n/a	n/a
50	CTCF	chr19:52104419-52104887	GM12891	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52104632-52104682	HEK293	kidney:	embryo
2	chr19:52102010-52102060	GM19239	blood:	n/a
3	chr19:52104997-52105047	HEK293	kidney:	embryo
4	chr19:52104632-52104682	HNPCEpiC	eye:	n/a
5	chr19:52104419-52104469	HPAEpiC	pulmonary alveolar:	n/a
6	chr19:52101874-52101924	SKMC	muscle:	n/a
7	chr19:52102023-52102073	Caco-2	colon:	n/a
8	chr19:52105721-52105771	PANC-1	pancreas:	n/a
9	chr19:52102010-52102060	HCT-116	colon:	n/a
10	chr19:52102010-52102060	GM12878	blood:	n/a
11	chr19:52101661-52101711	SK-N-SH	brain:	n/a
12	chr19:52099597-52099647	HEEpiC	esophagus:	n/a
13	chr19:52105721-52105771	SKMC	muscle:	n/a
14	chr19:52105721-52105771	HNPCEpiC	eye:	n/a
15	chr19:52104632-52104682	AG10803	skin:	n/a
16	chr19:52101874-52101924	AG04449	skin:	fetal
17	chr19:52102010-52102060	NB4	blood:	n/a
18	chr19:52102010-52102060	ProgFib	skin:	n/a
19	chr19:52102023-52102073	HPAEpiC	pulmonary alveolar:	n/a
20	chr19:52102010-52102060	HL-60	blood:	n/a
21	chr19:52104419-52104469	HCPEpiC	choroid plexus:	n/a
22	chr19:52099597-52099647	H1-hESC	embryonic stem cell:	embryo
23	chr19:52101661-52101711	GM12891	blood:	n/a
24	chr19:52101661-52101711	IMR90	lung:	fetal
25	chr19:52104997-52105047	HCM	heart:	n/a
26	chr19:52099597-52099647	HCM	heart:	n/a
27	chr19:52101661-52101711	AG09309	skin:	n/a
28	chr19:52105721-52105771	HAEpiC	amniotic membrane:	n/a
29	chr19:52104632-52104682	LNCaP	prostate:	n/a
30	chr19:52104632-52104682	HPAEpiC	pulmonary alveolar:	n/a
31	chr19:52099597-52099647	HPAEpiC	pulmonary alveolar:	n/a
32	chr19:52105721-52105771	BE2_C	brain:	n/a
33	chr19:52102023-52102073	AoSMC	blood vessel:	n/a
34	chr19:52105721-52105771	Hela-S3	cervix:	n/a
35	chr19:52102010-52102060	HMEC	breast:	n/a
36	chr19:52104632-52104682	K562	blood:	n/a
37	chr19:52104997-52105047	SK-N-SH_RA	brain:	n/a
38	chr19:52104419-52104469	U87	brain:	n/a
39	chr19:52104632-52104682	Caco-2	colon:	n/a
40	chr19:52104997-52105047	BE2_C	brain:	n/a
41	chr19:52104419-52104469	ovcar-3	ovarian:	n/a
42	chr19:52104997-52105047	MCF10A-Er-Src	breast:	n/a
43	chr19:52105721-52105771	HEK293	kidney:	embryo
44	chr19:52105721-52105771	NHDF-neo	bronchial:	n/a
45	chr19:52103425-52103475	AG09319	gingival:	n/a
46	chr19:52102023-52102073	HCT-116	colon:	n/a
47	chr19:52102010-52102060	ovcar-3	ovarian:	n/a
48	chr19:52104419-52104469	HRCEpiC	kidney:	n/a
49	chr19:52104997-52105047	NB4	blood:	n/a
50	chr19:52099597-52099647	A549	lung:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:52098792..52101789-chr19:52105276..52108057,2	K562	blood:
2	chr19:52073066..52077206-chr19:52096074..52099799,4	K562	blood:
3	chr19:52097772..52099435-chr19:52099519..52102447,4	K562	blood:
4	chr19:52101743..52103546-chr19:52105521..52108118,2	K562	blood:
5	chr19:52096005..52097791-chr19:52103717..52105932,2	K562	blood:
6	chr19:52095454..52097791-chr19:52104410..52105932,2	K562	blood:
7	chr19:52075666..52078013-chr19:52102124..52103680,2	K562	blood:
8	chr19:52097772..52099435-chr19:52099519..52102447,4	K562	blood:
9	chr19:52098792..52101789-chr19:52105276..52108057,2	K562	blood:
10	chr19:52097873..52100049-chr19:52100051..52101814,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF175-3	chr19:52104965-52104999	NONHSAT067455
2	lnc-ZNF175-3	chr19:52105456-52105735	NONHSAT067455
3	lnc-ZNF175-2	chr19:52102542-52103723	ENSG00000267808.1

No data

Variant related genes	Relation type
ENSG00000267808	TF binding region
ENSG00000269388	TF binding region
ENSG00000167765	TF binding region
ENSG00000267808	CpG island
ENSG00000269388	CpG island
ENSG00000167765	CpG island
ENSG00000269388	chromatin interactions
ENSG00000167765	chromatin interactions
ENSG00000267808	chromatin interactions
ENSG00000105497	chromatin interactions

Extended variants
information (count: 371 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561028632	chr19:52099362-52099363	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs28419240	chr19:52099435-52099436	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs529457479	chr19:52099443-52099444	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs12973225	chr19:52099452-52099453	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs536767622	chr19:52099457-52099458	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs61438598	chr19:52099472-52099473	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs78510393	chr19:52099562-52099563	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs12973066	chr19:52099568-52099569	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs4801880	chr19:52099648-52099649	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs4801881	chr19:52099662-52099663	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs76990050	chr19:52099669-52099670	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs78709884	chr19:52099674-52099675	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs12973120	chr19:52099687-52099688	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs191874088	chr19:52099710-52099711	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs367759885	chr19:52099715-52099716	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs183697497	chr19:52099716-52099717	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs12973346	chr19:52099721-52099722	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs563395544	chr19:52099752-52099753	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs554933455	chr19:52099766-52099767	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs543837472	chr19:52099811-52099812	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs562095482	chr19:52099834-52099835	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574595442	chr19:52099866-52099867	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs116798585	chr19:52099941-52099942	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs559817714	chr19:52099944-52099945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs4802822	chr19:52099985-52099986	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs114487398	chr19:52099988-52099989	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570002616	chr19:52100023-52100024	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs144679698	chr19:52100037-52100038	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548548140	chr19:52100051-52100052	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566956083	chr19:52100054-52100055	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs35936222	chr19:52100087-52100088	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187652757	chr19:52100092-52100093	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs190618375	chr19:52100099-52100100	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs538446309	chr19:52100102-52100103	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372052218	chr19:52100112-52100113	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs11878907	chr19:52100155-52100156	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs182775875	chr19:52100222-52100223	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs542980269	chr19:52100253-52100254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369374745	chr19:52100258-52100259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs561185213	chr19:52100261-52100262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs187101859	chr19:52100290-52100291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs11881852	chr19:52100325-52100326	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs559544606	chr19:52100326-52100327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs11879019	chr19:52100331-52100332	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs143246810	chr19:52100352-52100353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs145565506	chr19:52100353-52100354	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551678703	chr19:52100403-52100404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs369162149	chr19:52100415-52100416	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570340560	chr19:52100478-52100479	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs192741669	chr19:52100553-52100554	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52098400-52099400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr19:52098400-52101600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:52098400-52102000	Weak transcription	Right Atrium	heart
4	chr19:52098600-52099600	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr19:52098600-52099600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr19:52098600-52101400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr19:52098600-52101800	Weak transcription	Gastric	stomach
8	chr19:52098600-52101800	Weak transcription	Spleen	Spleen
9	chr19:52098600-52105000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr19:52098600-52110400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr19:52098800-52099400	Enhancers	Pancreas	Pancrea
12	chr19:52098800-52099600	Enhancers	K562	blood
13	chr19:52098800-52099800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr19:52098800-52101800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr19:52098800-52110600	Weak transcription	Brain Anterior Caudate	brain
16	chr19:52099400-52110800	Weak transcription	Pancreas	Pancrea
17	chr19:52101000-52101200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr19:52101400-52102000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr19:52101600-52102200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:52101800-52102000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr19:52101800-52102000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr19:52101800-52102000	Enhancers	Placenta	Placenta
23	chr19:52101800-52102000	Flanking Active TSS	Gastric	stomach
24	chr19:52101800-52102400	ZNF genes & repeats	Spleen	Spleen
25	chr19:52102000-52102200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr19:52102000-52102200	Active TSS	Gastric	stomach
27	chr19:52102000-52102400	Weak transcription	Primary B cells from peripheral blood	blood
28	chr19:52102200-52105400	Weak transcription	Gastric	stomach
29	chr19:52102400-52104200	Weak transcription	Spleen	Spleen
30	chr19:52102600-52103000	Enhancers	GM12878-XiMat	blood
31	chr19:52102600-52104200	Enhancers	Primary B cells from peripheral blood	blood
32	chr19:52103000-52103400	Active TSS	GM12878-XiMat	blood
33	chr19:52103400-52104600	Flanking Active TSS	GM12878-XiMat	blood
34	chr19:52104000-52104200	Bivalent Enhancer	Primary B cells from cord blood	blood
35	chr19:52104000-52104200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
36	chr19:52104000-52104200	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr19:52104000-52104400	Active TSS	Rectal Mucosa Donor 29	rectum
38	chr19:52104000-52104600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr19:52104000-52104800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
40	chr19:52104000-52105000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
41	chr19:52104000-52105800	Active TSS	Duodenum Mucosa	Duodenum
42	chr19:52104200-52104400	Flanking Active TSS	Primary B cells from cord blood	blood
43	chr19:52104200-52104400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
44	chr19:52104200-52104400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr19:52104200-52104400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr19:52104200-52104400	Bivalent Enhancer	Fetal Thymus	thymus
47	chr19:52104200-52104400	Bivalent/Poised TSS	Small Intestine	intestine
48	chr19:52104200-52104600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
49	chr19:52104200-52104600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
50	chr19:52104200-52104600	Flanking Active TSS	Primary B cells from peripheral blood	blood

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