Variant report

Variant	esv10933
Chromosome Location	chr19:45588911-45595377
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:589)
CpG islands
(count:366)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:45594722-45595142	K562	blood:	n/a	n/a
2	ATF2	chr19:45594226-45595423	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr19:45594659-45595398	GM12878	blood:	n/a	n/a
4	ATF2	chr19:45594690-45595375	GM12878	blood:	n/a	n/a
5	ATF2	chr19:45594467-45595320	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr19:45594403-45595528	A549	lung:	n/a	n/a
7	ATF3	chr19:45594530-45595398	A549	lung:	n/a	n/a
8	BCL3	chr19:45594094-45595510	A549	lung:	n/a	chr19:45594907-45594916
9	BCL3	chr19:45594831-45595261	GM12878	blood:	n/a	chr19:45594907-45594916
10	BCL3	chr19:45594716-45595251	GM12878	blood:	n/a	chr19:45594907-45594916
11	BCL3	chr19:45594035-45595581	A549	lung:	n/a	chr19:45594907-45594916
12	BCLAF1	chr19:45594691-45595274	GM12878	blood:	n/a	chr19:45594907-45594916
13	BCLAF1	chr19:45594593-45595426	GM12878	blood:	n/a	chr19:45594907-45594916
14	BHLHE40	chr19:45594795-45595272	GM12878	blood:	n/a	n/a
15	BHLHE40	chr19:45594289-45594592	K562	blood:	n/a	n/a
16	BHLHE40	chr19:45594861-45595145	K562	blood:	n/a	n/a
17	BRCA1	chr19:45594809-45595238	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr19:45594372-45595190	K562	blood:	n/a	n/a
19	CCNT2	chr19:45594780-45595105	K562	blood:	n/a	n/a
20	CEBPB	chr19:45592800-45592879	IMR90	lung:	n/a	n/a
21	CEBPB	chr19:45594928-45594978	K562	blood:	n/a	n/a
22	CEBPB	chr19:45594761-45595483	GM12878	blood:	n/a	n/a
23	CEBPB	chr19:45594825-45595300	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr19:45594734-45595250	GM12878	blood:	n/a	n/a
25	CHD2	chr19:45594726-45595172	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr19:45594964-45595118	K562	blood:	n/a	n/a
27	CREB1	chr19:45594655-45595266	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr19:45594757-45595226	ECC-1	luminal epithelium:	n/a	n/a
29	CREB1	chr19:45594681-45595255	A549	lung:	n/a	n/a
30	CREB1	chr19:45594591-45595319	GM12878	blood:	n/a	n/a
31	CREB1	chr19:45594766-45595206	A549	lung:	n/a	n/a
32	CREB1	chr19:45594296-45594675	A549	lung:	n/a	n/a
33	CREB1	chr19:45594488-45595416	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr19:45592600-45592750	RPTEC	kidney:	n/a	n/a
35	CTCF	chr19:45593373-45593525	HepG2	liver:	n/a	n/a
36	CTCF	chr19:45593371-45593584	HepG2	liver:	n/a	n/a
37	CTCF	chr19:45594380-45594530	SAEC	small airway:	n/a	n/a
38	CTCF	chr19:45593267-45593639	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr19:45592540-45592690	MCF-7	breast:	n/a	n/a
40	CTCF	chr19:45593436-45593522	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr19:45592600-45592750	AG10803	skin:	n/a	n/a
42	CTCF	chr19:45594445-45594466	MCF-7	breast:	n/a	n/a
43	CTCF	chr19:45594720-45594870	BJ	skin:	n/a	n/a
44	CTCF	chr19:45592560-45592710	HPF	lung:	n/a	n/a
45	CTCF	chr19:45592644-45592768	IMR90	lung:	n/a	n/a
46	CTCF	chr19:45592600-45592750	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr19:45592620-45592770	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr19:45592620-45592770	GM12873	blood:	n/a	n/a
49	CTCF	chr19:45594300-45594450	HRE	kidney:	n/a	n/a
50	CTCF	chr19:45593421-45593523	MCF-7	breast:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:45590882-45590932	HUVEC	blood vessel:	n/a
2	chr19:45593439-45593489	IMR90	lung:	fetal
3	chr19:45594670-45594720	H1-hESC	embryonic stem cell:	embryo
4	chr19:45594493-45594543	HIPEpiC	eye:	n/a
5	chr19:45594670-45594720	AG10803	skin:	n/a
6	chr19:45593439-45593489	AG04449	skin:	fetal
7	chr19:45594493-45594543	T-47D	breast:	n/a
8	chr19:45594410-45594460	SK-N-SH	brain:	n/a
9	chr19:45594670-45594720	NHDF-neo	bronchial:	n/a
10	chr19:45595006-45595056	AG04449	skin:	fetal
11	chr19:45595006-45595056	AoSMC	blood vessel:	n/a
12	chr19:45590882-45590932	HMEC	breast:	n/a
13	chr19:45593439-45593489	BJ	skin:	n/a
14	chr19:45595006-45595056	HIPEpiC	eye:	n/a
15	chr19:45593439-45593489	AG04450	lung:	fetal
16	chr19:45590882-45590932	BE2_C	brain:	n/a
17	chr19:45594493-45594543	AG10803	skin:	n/a
18	chr19:45594670-45594720	HPAEpiC	pulmonary alveolar:	n/a
19	chr19:45594670-45594720	GM12878	blood:	n/a
20	chr19:45594410-45594460	HMEC	breast:	n/a
21	chr19:45594410-45594460	T-47D	breast:	n/a
22	chr19:45590882-45590932	BJ	skin:	n/a
23	chr19:45594493-45594543	GM12891	blood:	n/a
24	chr19:45594493-45594543	GM19239	blood:	n/a
25	chr19:45590882-45590932	AoSMC	blood vessel:	n/a
26	chr19:45594670-45594720	HCPEpiC	choroid plexus:	n/a
27	chr19:45594410-45594460	HIPEpiC	eye:	n/a
28	chr19:45594410-45594460	PrEC	prostate:	n/a
29	chr19:45594493-45594543	HRPEpiC	eye:	n/a
30	chr19:45594410-45594460	NHDF-neo	bronchial:	n/a
31	chr19:45593439-45593489	HCT-116	colon:	n/a
32	chr19:45594670-45594720	AG09309	skin:	n/a
33	chr19:45590882-45590932	GM12892	blood:	n/a
34	chr19:45593439-45593489	GM19239	blood:	n/a
35	chr19:45595006-45595056	MCF10A-Er-Src	breast:	n/a
36	chr19:45594410-45594460	RPTEC	kidney:	n/a
37	chr19:45594493-45594543	HEEpiC	esophagus:	n/a
38	chr19:45593439-45593489	HCPEpiC	choroid plexus:	n/a
39	chr19:45595006-45595056	HUVEC	blood vessel:	n/a
40	chr19:45594670-45594720	ProgFib	skin:	n/a
41	chr19:45594670-45594720	Caco-2	colon:	n/a
42	chr19:45593439-45593489	HRCEpiC	kidney:	n/a
43	chr19:45595006-45595056	NB4	blood:	n/a
44	chr19:45594410-45594460	A549	lung:	n/a
45	chr19:45590882-45590932	AG09319	gingival:	n/a
46	chr19:45594410-45594460	HCT-116	colon:	n/a
47	chr19:45594670-45594720	ovcar-3	ovarian:	n/a
48	chr19:45594670-45594720	IMR90	lung:	fetal
49	chr19:45593439-45593489	A549	lung:	n/a
50	chr19:45594670-45594720	NHBE	bronchial:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:45503630..45506563-chr19:45593514..45596516,3	MCF-7	breast:
2	chr19:45580763..45587822-chr19:45593153..45598212,14	K562	blood:
3	chr19:45595033..45597870-chr19:45646652..45650476,4	MCF-7	breast:
4	chr19:45594586..45596499-chr19:45682181..45685187,4	MCF-7	breast:
5	chr19:45571923..45576077-chr19:45594481..45600071,10	MCF-7	breast:
6	chr1:201951628..201952557-chr19:45594631..45595384,2	Hela-S3	cervix:
7	chr19:45576493..45586900-chr19:45588536..45604492,49	MCF-7	breast:
8	chr19:45593518..45596472-chr19:45847951..45849641,2	MCF-7	breast:
9	chr19:45570935..45574142-chr19:45593620..45597765,5	MCF-7	breast:
10	chr19:45592609..45593296-chr19:45634052..45635005,2	MCF-7	breast:
11	chr19:45577259..45585589-chr19:45592358..45603656,27	K562	blood:
12	chr19:45588372..45591369-chr19:45593427..45597756,7	K562	blood:
13	chr19:45576986..45585099-chr19:45592126..45598719,16	MCF-7	breast:
14	chr19:45503629..45506931-chr19:45593767..45597738,4	K562	blood:
15	chr19:45588372..45592155-chr19:45593848..45596718,4	K562	blood:
16	chr19:45594891..45596500-chr19:45754008..45755786,2	MCF-7	breast:
17	chr19:45588065..45589606-chr19:45593276..45595893,2	MCF-7	breast:
18	chr19:45594874..45597676-chr19:45681810..45683655,2	K562	blood:
19	chr19:45542175..45544773-chr19:45593754..45596386,2	MCF-7	breast:
20	chr19:45250268..45252334-chr19:45593239..45597540,3	MCF-7	breast:
21	chr19:45594892..45596535-chr19:45681783..45683354,2	MCF-7	breast:
22	chr19:45594755..45598539-chr19:45681810..45685400,4	K562	blood:
23	chr19:45542295..45544069-chr19:45594724..45597616,3	MCF-7	breast:
24	chr19:45588352..45590058-chr19:45595419..45597660,2	MCF-7	breast:
25	chr19:45394111..45396115-chr19:45593226..45596136,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R37-1	chr19:45595050-45595415	NONHSAT066758

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GEMIN7	hsa-let-7b-5p	chr19:45593969-45593990
2	GEMIN7	hsa-let-7b-5p	chr19:45593983-45593990

Variant related genes	Relation type
ENSG00000267348	TF binding region
PPP1R37	TF binding region
ENSG00000267348	CpG island
PPP1R37	CpG island
ENSG00000104856	chromatin interactions
ENSG00000267348	chromatin interactions
ENSG00000142252	chromatin interactions
ENSG00000130204	chromatin interactions
ENSG00000007047	chromatin interactions
ENSG00000069399	chromatin interactions
ENSG00000104859	chromatin interactions
ENSG00000170684	chromatin interactions
ENSG00000189114	chromatin interactions
ENSG00000176393	chromatin interactions
ENSG00000104866	chromatin interactions
ENSG00000267545	chromatin interactions
ENSG00000104892	chromatin interactions
ENSG00000267282	chromatin interactions

Extended variants
information (count: 278 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183799170	chr19:45588958-45588959	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs71298765	chr19:45588969-45588970	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs6509184	chr19:45588973-45588974	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs527299974	chr19:45588975-45588976	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs547378455	chr19:45588994-45588995	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs561573126	chr19:45589008-45589009	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs6509185	chr19:45589013-45589014	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs35415252	chr19:45589078-45589079	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs6509187	chr19:45589079-45589080	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs377298458	chr19:45589087-45589088	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs539149295	chr19:45589097-45589098	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs552410372	chr19:45589148-45589149	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs113506339	chr19:45589165-45589166	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs577475884	chr19:45589179-45589180	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs565800935	chr19:45589182-45589183	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs534705278	chr19:45589206-45589207	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs554494894	chr19:45589208-45589209	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs369854828	chr19:45589251-45589252	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs540043131	chr19:45589258-45589259	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs147410727	chr19:45589259-45589260	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs189159147	chr19:45589360-45589361	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs190762132	chr19:45589376-45589377	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs545155981	chr19:45589405-45589406	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs11671277	chr19:45589415-45589416	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs145311329	chr19:45589416-45589417	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs182339563	chr19:45589417-45589418	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs552174301	chr19:45589421-45589422	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs147244578	chr19:45589435-45589436	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs570179912	chr19:45589450-45589451	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs530461926	chr19:45589452-45589453	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs550182131	chr19:45589491-45589492	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs537560712	chr19:45589502-45589503	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs8105963	chr19:45589528-45589529	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs76353913	chr19:45589539-45589540	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs1469704	chr19:45589595-45589596	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs565837902	chr19:45589601-45589602	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs373362755	chr19:45589626-45589627	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs139713267	chr19:45589665-45589666	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs548217313	chr19:45589669-45589670	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs568091991	chr19:45589726-45589727	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs537425592	chr19:45589766-45589767	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs556200955	chr19:45589791-45589792	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs569892397	chr19:45589812-45589813	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs186694859	chr19:45589820-45589821	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs149774153	chr19:45589847-45589848	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs78072155	chr19:45589861-45589862	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs191500875	chr19:45589876-45589877	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs541108711	chr19:45589897-45589898	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs558420332	chr19:45589979-45589980	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs12975848	chr19:45590004-45590005	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	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
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Adrenocortical carcinoma	18281524	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Muscular dystrophy	17160897	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45583600-45593800	Weak transcription	Fetal Kidney	kidney
2	chr19:45583600-45594400	Weak transcription	Aorta	Aorta
3	chr19:45583600-45594600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr19:45583600-45595200	Weak transcription	Small Intestine	intestine
5	chr19:45583800-45593400	Weak transcription	Pancreas	Pancrea
6	chr19:45583800-45593600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr19:45583800-45594200	Weak transcription	Psoas Muscle	Psoas
8	chr19:45583800-45594400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr19:45584000-45594400	Weak transcription	Hela-S3	cervix
10	chr19:45584200-45594200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr19:45584200-45594200	Weak transcription	NH-A	brain
12	chr19:45584400-45589800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr19:45584400-45590000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr19:45584400-45590600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr19:45584400-45590600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr19:45584400-45590600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr19:45584400-45590600	Weak transcription	Fetal Brain Male	brain
18	chr19:45584400-45591400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr19:45584400-45593000	Strong transcription	Fetal Intestine Small	intestine
20	chr19:45584400-45593200	Weak transcription	Colonic Mucosa	Colon
21	chr19:45584400-45593600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr19:45584400-45593800	Weak transcription	Fetal Heart	heart
23	chr19:45584400-45593800	Strong transcription	Fetal Muscle Leg	muscle
24	chr19:45584400-45593800	Strong transcription	Fetal Stomach	stomach
25	chr19:45584400-45594000	Weak transcription	Stomach Mucosa	stomach
26	chr19:45584400-45594200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr19:45584600-45592400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr19:45584800-45593800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr19:45584800-45594000	Strong transcription	Fetal Muscle Trunk	muscle
30	chr19:45585600-45593200	Weak transcription	Ovary	ovary
31	chr19:45585600-45594200	Weak transcription	Primary B cells from cord blood	blood
32	chr19:45585800-45589800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr19:45585800-45591600	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr19:45585800-45591600	Weak transcription	Brain Angular Gyrus	brain
35	chr19:45585800-45593200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr19:45585800-45593200	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr19:45585800-45593200	Weak transcription	Brain Germinal Matrix	brain
38	chr19:45585800-45593200	Weak transcription	HSMMtube	muscle
39	chr19:45585800-45593400	Weak transcription	Fetal Lung	lung
40	chr19:45585800-45593400	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr19:45585800-45593400	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr19:45585800-45594000	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr19:45585800-45594000	Weak transcription	Colon Smooth Muscle	Colon
44	chr19:45585800-45594200	Weak transcription	Esophagus	oesophagus
45	chr19:45585800-45594600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr19:45586000-45589600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr19:45586000-45589600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr19:45586000-45589600	Weak transcription	Lung	lung
49	chr19:45586000-45589600	Weak transcription	Right Ventricle	heart
50	chr19:45586000-45590600	Weak transcription	Primary monocytes fromperipheralblood	blood

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