Variant report

Variant	esv3442638
Chromosome Location	chr19:55794165-55797013
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:54)
CpG islands
(count:428)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:54 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr19:55795170-55795467	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr19:55795286-55795549	K562	blood:	n/a	n/a
3	BRCA1	chr19:55794995-55795040	GM12878	blood:	n/a	n/a
4	CREB1	chr19:55795237-55795434	A549	lung:	n/a	n/a
5	CREB1	chr19:55795297-55795582	A549	lung:	n/a	n/a
6	CREB1	chr19:55795135-55795567	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr19:55796820-55796970	HCPEpiC	choroid plexus:	n/a	n/a
8	E2F6	chr19:55795299-55795420	K562	blood:	n/a	n/a
9	EGR1	chr19:55795286-55795523	K562	blood:	n/a	n/a
10	EGR1	chr19:55795296-55795546	K562	blood:	n/a	n/a
11	HDAC2	chr19:55795192-55795445	K562	blood:	n/a	n/a
12	JUND	chr19:55795261-55795417	H1-hESC	embryonic stem cell:	n/a	n/a
13	JUND	chr19:55795209-55795507	K562	blood:	n/a	n/a
14	MAX	chr19:55795164-55795577	SK-N-SH	brain:	n/a	n/a
15	MAX	chr19:55795283-55795426	K562	blood:	n/a	n/a
16	MAZ	chr19:55795101-55795688	K562	blood:	n/a	n/a
17	MAZ	chr19:55794951-55797382	IMR90	lung:	n/a	chr19:55795773-55795783
18	MAZ	chr19:55795498-55795502	GM12878	blood:	n/a	n/a
19	MYC	chr19:55795351-55795435	K562	blood:	n/a	n/a
20	MYC	chr19:55796111-55796114	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr19:55794853-55795460	U87	brain:	n/a	n/a
22	POLR2A	chr19:55795293-55795510	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr19:55795327-55795457	A549	lung:	n/a	n/a
24	POLR2A	chr19:55795777-55796168	H1-neurons	neurons:	n/a	n/a
25	POLR2A	chr19:55794871-55795717	H1-neurons	neurons:	n/a	n/a
26	POLR2A	chr19:55795862-55795871	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr19:55795372-55795426	K562	blood:	n/a	n/a
28	POLR2A	chr19:55794893-55795706	H1-neurons	neurons:	n/a	n/a
29	POLR2A	chr19:55795008-55795306	U87	brain:	n/a	n/a
30	POLR2A	chr19:55795297-55795491	HCT-116	colon:	n/a	n/a
31	POLR2A	chr19:55795857-55796052	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr19:55795807-55795840	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr19:55795878-55796151	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr19:55795292-55795638	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr19:55795250-55795531	HCT-116	colon:	n/a	n/a
36	RCOR1	chr19:55795020-55795454	K562	blood:	n/a	n/a
37	RCOR1	chr19:55795134-55795334	K562	blood:	n/a	n/a
38	REST	chr19:55794634-55796279	H1-neurons	neurons:	n/a	chr19:55795633-55795653 chr19:55795468-55795481 chr19:55795625-55795638 chr19:55795512-55795525 chr19:55795613-55795626
39	REST	chr19:55795288-55795421	SK-N-SH	brain:	n/a	n/a
40	SIN3A	chr19:55796007-55796084	H1-hESC	embryonic stem cell:	n/a	n/a
41	SP4	chr19:55795198-55795425	H1-hESC	embryonic stem cell:	n/a	n/a
42	TAF1	chr19:55795190-55795458	H1-hESC	embryonic stem cell:	n/a	n/a
43	TAF1	chr19:55794884-55795375	H1-neurons	neurons:	n/a	n/a
44	TAF1	chr19:55795280-55795480	SK-N-SH	brain:	n/a	n/a
45	TCF7L2	chr19:55795038-55795067	Hela-S3	cervix:	n/a	n/a
46	YY1	chr19:55795117-55795371	H1-hESC	embryonic stem cell:	n/a	n/a
47	YY1	chr19:55795216-55795483	HCT-116	colon:	n/a	n/a
48	YY1	chr19:55795302-55795407	K562	blood:	n/a	n/a
49	ZBTB7A	chr19:55795138-55795666	ECC-1	luminal epithelium:	n/a	chr19:55795563-55795571
50	ZBTB7A	chr19:55795244-55795593	K562	blood:	n/a	chr19:55795563-55795571

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:55795815-55795865	HRCEpiC	kidney:	n/a
2	chr19:55795815-55795865	HRCEpiC	kidney:	n/a
3	chr19:55795571-55795621	AG04450	lung:	fetal
4	chr19:55795380-55795430	NB4	blood:	n/a
5	chr19:55795380-55795430	U87	brain:	n/a
6	chr19:55795571-55795621	SK-N-MC	brain:	n/a
7	chr19:55795459-55795509	SAEC	small airway:	n/a
8	chr19:55794478-55794528	ovcar-3	ovarian:	n/a
9	chr19:55794478-55794528	HRCEpiC	kidney:	n/a
10	chr19:55795380-55795430	GM12878	blood:	n/a
11	chr19:55794444-55794494	GM12892	blood:	n/a
12	chr19:55795459-55795509	A549	lung:	n/a
13	chr19:55794444-55794494	AG09319	gingival:	n/a
14	chr19:55795459-55795509	HUVEC	blood vessel:	n/a
15	chr19:55794597-55794647	BE2_C	brain:	n/a
16	chr19:55795459-55795509	SK-N-SH_RA	brain:	n/a
17	chr19:55794478-55794528	NB4	blood:	n/a
18	chr19:55795571-55795621	MCF-7	breast:	n/a
19	chr19:55795459-55795509	CMK	blood:	n/a
20	chr19:55794597-55794647	U87	brain:	n/a
21	chr19:55795815-55795865	NHBE	bronchial:	n/a
22	chr19:55795815-55795865	CMK	blood:	n/a
23	chr19:55794478-55794528	GM12878	blood:	n/a
24	chr19:55794444-55794494	PANC-1	pancreas:	n/a
25	chr19:55794597-55794647	NB4	blood:	n/a
26	chr19:55794444-55794494	AG09309	skin:	n/a
27	chr19:55795815-55795865	GM12891	blood:	n/a
28	chr19:55795571-55795621	HL-60	blood:	n/a
29	chr19:55795571-55795621	ovcar-3	ovarian:	n/a
30	chr19:55795571-55795621	PFSK-1	brain:	n/a
31	chr19:55795459-55795509	NB4	blood:	n/a
32	chr19:55795571-55795621	Caco-2	colon:	n/a
33	chr19:55794444-55794494	AoSMC	blood vessel:	n/a
34	chr19:55795815-55795865	AG09309	skin:	n/a
35	chr19:55794478-55794528	IMR90	lung:	fetal
36	chr19:55795815-55795865	LNCaP	prostate:	n/a
37	chr19:55795380-55795430	PrEC	prostate:	n/a
38	chr19:55795380-55795430	MCF-7	breast:	n/a
39	chr19:55795815-55795865	HPAEpiC	pulmonary alveolar:	n/a
40	chr19:55795815-55795865	ovcar-3	ovarian:	n/a
41	chr19:55794444-55794494	ECC-1	luminal epithelium:	n/a
42	chr19:55794597-55794647	AG04449	skin:	fetal
43	chr19:55795815-55795865	NT2-D1	testis:	n/a
44	chr19:55794444-55794494	HRPEpiC	eye:	n/a
45	chr19:55794444-55794494	SK-N-MC	brain:	n/a
46	chr19:55794444-55794494	Caco-2	colon:	n/a
47	chr19:55795459-55795509	HRE	kidney:	n/a
48	chr19:55795459-55795509	HRPEpiC	eye:	n/a
49	chr19:55795380-55795430	Caco-2	colon:	n/a
50	chr19:55795380-55795430	HIPEpiC	eye:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:55793274..55795541-chr19:55812526..55814100,2	MCF-7	breast:
2	chr19:55794940..55798200-chr19:55895681..55898839,3	K562	blood:
3	chr19:55788649..55794261-chr19:55847636..55852828,10	K562	blood:
4	chr19:55787879..55795650-chr19:55893762..55898931,9	MCF-7	breast:
5	chr19:55795553..55797750-chr19:55917635..55920428,2	MCF-7	breast:
6	chr19:55790346..55793216-chr19:55794114..55797002,3	MCF-7	breast:
7	chr19:55789007..55794976-chr19:55917716..55921043,9	K562	blood:
8	chr19:55768870..55771541-chr19:55794018..55795820,2	MCF-7	breast:
9	chr19:55764275..55774774-chr19:55790059..55800763,24	K562	blood:
10	chr19:55725965..55728542-chr19:55794758..55796322,2	K562	blood:
11	chr19:55795849..55798225-chr19:55800682..55803471,3	K562	blood:
12	chr19:55790016..55797764-chr19:55893451..55899813,15	MCF-7	breast:

No data

Variant related genes	Relation type
HSPBP1	TF binding region
BRSK1	TF binding region
HSPBP1	CpG island
BRSK1	CpG island
ENSG00000105063	chromatin interactions
ENSG00000133247	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000108107	chromatin interactions
ENSG00000160469	chromatin interactions
ENSG00000267649	chromatin interactions
ENSG00000133265	chromatin interactions
ENSG00000267531	chromatin interactions
ENSG00000233493	chromatin interactions

Extended variants
information (count: 102 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:102 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548089322	chr19:55794188-55794189	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs567968143	chr19:55794218-55794219	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs534043379	chr19:55794228-55794229	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs553678954	chr19:55794242-55794243	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs577303463	chr19:55794250-55794251	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs62126357	chr19:55794266-55794267	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs556658797	chr19:55794286-55794287	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs28412279	chr19:55794293-55794294	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs542195540	chr19:55794310-55794311	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs562412592	chr19:55794336-55794337	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs192015663	chr19:55794345-55794346	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs552564598	chr19:55794363-55794364	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs148602192	chr19:55794391-55794392	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs564498835	chr19:55794433-55794434	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs75068893	chr19:55794439-55794440	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs552882936	chr19:55794462-55794463	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs373815857	chr19:55794478-55794479	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs551871344	chr19:55794479-55794480	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS	CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs562205022	chr19:55794651-55794652	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs531209737	chr19:55794657-55794658	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs547782324	chr19:55794694-55794695	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs568385884	chr19:55794697-55794698	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs533832335	chr19:55794743-55794744	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs371645910	chr19:55794826-55794827	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs566325755	chr19:55794852-55794853	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs182754355	chr19:55794918-55794919	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs201544128	chr19:55795029-55795030	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs138183711	chr19:55795030-55795031	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs368345093	chr19:55795031-55795032	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs111062016	chr19:55795033-55795034	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs570568634	chr19:55795044-55795045	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs151157122	chr19:55795054-55795055	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs75670219	chr19:55795063-55795064	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs576605997	chr19:55795093-55795094	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs535892562	chr19:55795138-55795139	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs367984852	chr19:55795190-55795191	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs555781597	chr19:55795192-55795193	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs143100136	chr19:55795213-55795214	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs572725282	chr19:55795230-55795231	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs34060285	chr19:55795266-55795267	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs541381005	chr19:55795319-55795320	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs528022078	chr19:55795406-55795407	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs558397169	chr19:55795433-55795434	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs578117523	chr19:55795493-55795494	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs112122019	chr19:55795509-55795510	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs113969703	chr19:55795536-55795537	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs543563139	chr19:55795657-55795658	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs562289626	chr19:55795748-55795749	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs201695409	chr19:55795758-55795759	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs531300262	chr19:55795791-55795792	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD

Chromatin state (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55791600-55796000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr19:55791800-55795000	Weak transcription	HSMMtube	muscle
3	chr19:55791800-55796600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr19:55792000-55795000	Weak transcription	HSMM	muscle
5	chr19:55792200-55794400	Weak transcription	Fetal Brain Male	brain
6	chr19:55792200-55794600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr19:55792200-55794800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr19:55792200-55795000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr19:55792200-55795000	Weak transcription	Aorta	Aorta
10	chr19:55792200-55795000	Weak transcription	Right Atrium	heart
11	chr19:55792200-55795000	Weak transcription	NH-A	brain
12	chr19:55792400-55794400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr19:55792400-55794400	Weak transcription	Brain Anterior Caudate	brain
14	chr19:55792400-55794400	Weak transcription	Brain Germinal Matrix	brain
15	chr19:55792400-55794400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr19:55792400-55794600	Weak transcription	Primary T cells from cord blood	blood
17	chr19:55792400-55794600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr19:55792400-55794600	Weak transcription	Brain Hippocampus Middle	brain
19	chr19:55792400-55794600	Weak transcription	Brain Substantia Nigra	brain
20	chr19:55792400-55794600	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr19:55792400-55794800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr19:55792400-55794800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr19:55792400-55795000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr19:55792400-55795000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr19:55792400-55795000	Weak transcription	Fetal Muscle Trunk	muscle
26	chr19:55792400-55795000	Weak transcription	Dnd41	blood
27	chr19:55792400-55795600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr19:55792400-55796800	Weak transcription	Gastric	stomach
29	chr19:55792400-55797000	Weak transcription	Pancreas	Pancrea
30	chr19:55792600-55794400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr19:55792600-55794400	Weak transcription	Brain Angular Gyrus	brain
32	chr19:55792600-55794400	Weak transcription	Brain Cingulate Gyrus	brain
33	chr19:55792600-55794600	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr19:55792600-55794800	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr19:55792600-55794800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr19:55792600-55794800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr19:55792600-55794800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr19:55792600-55794800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr19:55792600-55794800	Weak transcription	Colon Smooth Muscle	Colon
40	chr19:55792600-55794800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr19:55792600-55794800	Weak transcription	Fetal Heart	heart
42	chr19:55792600-55794800	Weak transcription	Stomach Smooth Muscle	stomach
43	chr19:55792600-55795000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr19:55792600-55795000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr19:55792600-55795000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr19:55792600-55795000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr19:55792600-55795000	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr19:55792600-55795000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr19:55792600-55795000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr19:55792600-55795000	Weak transcription	Fetal Kidney	kidney

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