Variant report

Variant	esv3334156
Chromosome Location	chr19:23590778-23742435
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1235)
CpG islands
(count:488)
Chromatin interactive
region (count:9)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1235 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:23592964-23593248	HepG2	liver:	n/a	n/a
2	ATF1	chr19:23632171-23632277	K562	blood:	n/a	n/a
3	BACH1	chr19:23665785-23666020	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr19:23598347-23598392	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr19:23623769-23623831	HepG2	liver:	n/a	n/a
6	BRCA1	chr19:23598769-23598984	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr19:23737404-23737655	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr19:23703034-23704567	HepG2	liver:	n/a	n/a
9	CEBPB	chr19:23683213-23683393	HepG2	liver:	n/a	chr19:23683224-23683235
10	CEBPB	chr19:23644231-23644824	Hela-S3	cervix:	n/a	chr19:23644704-23644715
11	CEBPB	chr19:23737273-23737956	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr19:23590403-23591203	HepG2	liver:	n/a	n/a
13	CEBPB	chr19:23714492-23714717	IMR90	lung:	n/a	chr19:23714556-23714567
14	CEBPB	chr19:23590509-23591131	A549	lung:	n/a	n/a
15	CEBPB	chr19:23726192-23726392	A549	lung:	n/a	n/a
16	CEBPB	chr19:23702877-23703664	A549	lung:	n/a	n/a
17	CEBPB	chr19:23714110-23714827	HepG2	liver:	n/a	chr19:23714556-23714567
18	CEBPB	chr19:23707275-23707432	HepG2	liver:	n/a	n/a
19	CEBPB	chr19:23641049-23641085	HepG2	liver:	n/a	n/a
20	CEBPB	chr19:23646302-23646762	HepG2	liver:	n/a	n/a
21	CEBPB	chr19:23722270-23722731	MCF-7	breast:	n/a	n/a
22	CEBPB	chr19:23644084-23644837	A549	lung:	n/a	chr19:23644704-23644715
23	CEBPB	chr19:23590437-23591084	IMR90	lung:	n/a	n/a
24	CEBPB	chr19:23728072-23728616	A549	lung:	n/a	n/a
25	CEBPB	chr19:23643222-23643770	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:23705193-23705662	MCF-7	breast:	n/a	n/a
27	CEBPB	chr19:23590897-23591117	K562	blood:	n/a	n/a
28	CEBPB	chr19:23705280-23705623	IMR90	lung:	n/a	n/a
29	CEBPB	chr19:23590450-23591152	HepG2	liver:	n/a	n/a
30	CEBPB	chr19:23726629-23726742	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:23644241-23644836	IMR90	lung:	n/a	chr19:23644704-23644715
32	CEBPB	chr19:23705291-23705718	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr19:23728287-23728951	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:23705300-23705591	HepG2	liver:	n/a	n/a
35	CEBPB	chr19:23726968-23727205	A549	lung:	n/a	chr19:23727071-23727082
36	CEBPB	chr19:23644538-23644861	HepG2	liver:	n/a	chr19:23644704-23644715
37	CEBPB	chr19:23705244-23705712	A549	lung:	n/a	n/a
38	CEBPB	chr19:23705258-23705669	MCF-7	breast:	n/a	n/a
39	CEBPB	chr19:23702925-23703368	IMR90	lung:	n/a	n/a
40	CEBPB	chr19:23714324-23714886	Hela-S3	cervix:	n/a	chr19:23714556-23714567
41	CEBPB	chr19:23641566-23642084	A549	lung:	n/a	chr19:23641688-23641699
42	CEBPB	chr19:23683187-23683291	K562	blood:	n/a	chr19:23683224-23683235
43	CEBPB	chr19:23742064-23742103	HepG2	liver:	n/a	n/a
44	CEBPB	chr19:23590358-23590849	MCF-7	breast:	n/a	n/a
45	CEBPB	chr19:23641669-23642085	IMR90	lung:	n/a	chr19:23641688-23641699
46	CEBPB	chr19:23726983-23727207	IMR90	lung:	n/a	chr19:23727071-23727082
47	CEBPB	chr19:23718314-23718394	HepG2	liver:	n/a	chr19:23718378-23718389
48	CEBPB	chr19:23726285-23726403	HepG2	liver:	n/a	n/a
49	CEBPB	chr19:23714085-23714861	A549	lung:	n/a	chr19:23714556-23714567
50	CEBPB	chr19:23641575-23642271	HepG2	liver:	n/a	chr19:23641688-23641699

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:23657425-23657475	HEEpiC	esophagus:	n/a
2	chr19:23654159-23654209	AoSMC	blood vessel:	n/a
3	chr19:23657425-23657475	HCM	heart:	n/a
4	chr19:23654159-23654209	SKMC	muscle:	n/a
5	chr19:23657425-23657475	SAEC	small airway:	n/a
6	chr19:23657425-23657475	GM06990	blood:	n/a
7	chr19:23654274-23654324	A549	lung:	n/a
8	chr19:23654159-23654209	HUVEC	blood vessel:	n/a
9	chr19:23653996-23654046	AG09319	gingival:	n/a
10	chr19:23657425-23657475	GM12892	blood:	n/a
11	chr19:23657425-23657475	SK-N-MC	brain:	n/a
12	chr19:23654159-23654209	A549	lung:	n/a
13	chr19:23653200-23653250	HEEpiC	esophagus:	n/a
14	chr19:23653996-23654046	SKMC	muscle:	n/a
15	chr19:23653996-23654046	NB4	blood:	n/a
16	chr19:23653200-23653250	GM06990	blood:	n/a
17	chr19:23653996-23654046	BJ	skin:	n/a
18	chr19:23654227-23654277	GM06990	blood:	n/a
19	chr19:23653200-23653250	ProgFib	skin:	n/a
20	chr19:23657425-23657475	U87	brain:	n/a
21	chr19:23653200-23653250	ovcar-3	ovarian:	n/a
22	chr19:23654274-23654324	ECC-1	luminal epithelium:	n/a
23	chr19:23657425-23657475	SKMC	muscle:	n/a
24	chr19:23654274-23654324	IMR90	lung:	fetal
25	chr19:23598854-23598904	HepG2	liver:	n/a
26	chr19:23657425-23657475	MCF10A-Er-Src	breast:	n/a
27	chr19:23654227-23654277	NHBE	bronchial:	n/a
28	chr19:23654159-23654209	IMR90	lung:	fetal
29	chr19:23653837-23653887	GM06990	blood:	n/a
30	chr19:23598854-23598904	HCM	heart:	n/a
31	chr19:23654159-23654209	HEK293	kidney:	embryo
32	chr19:23657425-23657475	RPTEC	kidney:	n/a
33	chr19:23654159-23654209	HIPEpiC	eye:	n/a
34	chr19:23654227-23654277	Caco-2	colon:	n/a
35	chr19:23653200-23653250	HIPEpiC	eye:	n/a
36	chr19:23653837-23653887	GM12878	blood:	n/a
37	chr19:23653996-23654046	Jurkat	blood:	n/a
38	chr19:23653837-23653887	HCF	heart:	n/a
39	chr19:23653996-23654046	PFSK-1	brain:	n/a
40	chr19:23653200-23653250	HL-60	blood:	n/a
41	chr19:23653996-23654046	SK-N-MC	brain:	n/a
42	chr19:23654274-23654324	AG09309	skin:	n/a
43	chr19:23654274-23654324	GM19239	blood:	n/a
44	chr19:23654274-23654324	HPAEpiC	pulmonary alveolar:	n/a
45	chr19:23654159-23654209	RPTEC	kidney:	n/a
46	chr19:23654159-23654209	Caco-2	colon:	n/a
47	chr19:23654159-23654209	HL-60	blood:	n/a
48	chr19:23654227-23654277	A549	lung:	n/a
49	chr19:23654274-23654324	AG04450	lung:	fetal
50	chr19:23653837-23653887	PrEC	prostate:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:23716991..23718899-chr19:23719198..23721188,2	MCF-7	breast:
2	chr19:23598116..23599107-chr19:24216116..24216947,3	MCF-7	breast:
3	chr19:23716991..23718899-chr19:23719198..23721188,2	MCF-7	breast:
4	chr19:23597107..23600085-chr19:24215651..24217575,2	MCF-7	breast:
5	chr19:23576617..23579164-chr19:23594549..23597394,2	MCF-7	breast:
6	chr19:23675218..23675970-chr2:239597148..239597648,2	NB4	blood:
7	chr19:23598106..23598617-chr19:24216264..24217103,2	MCF-7	breast:
8	chr19:23597097..23600084-chr19:24215418..24217838,2	MCF-7	breast:
9	chr19:23598051..23598951-chr19:24216258..24216783,2	NB4	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF91-1	chr19:23598696-23598903	NONHSAT063906
2	lnc-ZNF91-3	chr19:23688077-23688167	NONHSAT063921
3	lnc-RPSAP58-1	chr19:23741124-23741230	XLOC_013022
4	lnc-ZNF91-1	chr19:23590700-23590900	NONHSAT063908
5	lnc-ZNF675-1	chr19:23714333-23714492	XLOC_013278
6	lnc-ZNF91-1	chr19:23598696-23598867	ENSG00000269416.1
7	lnc-ZNF91-1	chr19:23590700-23590893	ENSG00000269416.1
8	lnc-ZNF675-1	chr19:23710720-23710821	NONHSAT063926
9	lnc-ZNF675-1	chr19:23708876-23709389	NONHSAT063926
10	lnc-ZNF730-16	chr19:23627064-23627991	NONHSAT063920
11	lnc-ZNF91-1	chr19:23598696-23598873	ENSG00000269416.1
12	lnc-ZNF91-1	chr19:23598706-23598876	ENSG00000269416.1
13	lnc-RPSAP58-1	chr19:23740397-23740511	XLOC_013022
14	lnc-ZNF91-3	chr19:23680678-23680837	NONHSAT063921
15	lnc-ZNF91-1	chr19:23598706-23598867	ENSG00000269416.1
16	lnc-ZNF675-1	chr19:23710720-23710816	XLOC_013278
17	lnc-ZNF91-1	chr19:23598696-23598849	ENSG00000269416.1
18	lnc-ZNF675-1	chr19:23708550-23709389	XLOC_013278
19	lnc-ZNF91-1	chr19:23598696-23598873	ENSG00000246181
20	lnc-ZNF675-1	chr19:23708438-23709389	XLOC_013278
21	lnc-ZNF91-1	chr19:23590700-23590900	ENSG00000246181
22	lnc-ZNF91-1	chr19:23598706-23598876	ENSG00000269416.1
23	lnc-ZNF730-15	chr19:23621816-23621921	NONHSAT063919
24	lnc-ZNF730-15	chr19:23622367-23622744	NONHSAT063919
25	lnc-ZNF91-1	chr19:23598696-23598861	ENSG00000269416.1
26	lnc-ZNF675-1	chr19:23710720-23710816	XLOC_013278
27	lnc-RPSAP58-1	chr19:23734519-23734611	XLOC_013022
28	lnc-RPSAP58-1	chr19:23741124-23741642	XLOC_013022
29	lnc-ZNF91-1	chr19:23598696-23598877	ENSG00000269416.1

No data

Variant related genes	Relation type
ZNF725P	TF binding region
VN1R92P	TF binding region
ENSG00000269416	TF binding region
ZNF725P	CpG island
VN1R92P	CpG island
ENSG00000269416	CpG island
ENSG00000268362	chromatin interactions
ENSG00000213096	chromatin interactions
ENSG00000167232	chromatin interactions
GTF2IRD2	miRNA target sites
NEO1	miRNA target sites
RAB34	miRNA target sites
USP6NL	miRNA target sites
MASTL	miRNA target sites
CYR61	miRNA target sites
SP4	miRNA target sites
SKIV2L2	miRNA target sites

Extended variants
information (count: 4011 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:4011 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533872251	chr19:23590782-23590783	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
2	rs546386692	chr19:23590791-23590792	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
3	rs532597953	chr19:23590800-23590801	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
4	rs144210645	chr19:23590804-23590805	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs369391393	chr19:23590805-23590806	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs569077567	chr19:23590864-23590865	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs530334920	chr19:23590876-23590877	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs373648048	chr19:23590886-23590887	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs548549780	chr19:23590918-23590919	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs564661772	chr19:23590938-23590939	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs553644861	chr19:23590947-23590948	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs190275143	chr19:23591059-23591060	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs112463166	chr19:23591060-23591061	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs533929097	chr19:23591063-23591064	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs559043453	chr19:23591064-23591065	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs141299425	chr19:23591079-23591080	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs538313910	chr19:23591165-23591166	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs367965127	chr19:23591181-23591182	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs112072369	chr19:23591217-23591218	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11882160	chr19:23591226-23591227	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs542990626	chr19:23591244-23591245	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555597167	chr19:23591251-23591252	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182480496	chr19:23591261-23591262	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572831027	chr19:23591267-23591268	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs13346220	chr19:23591273-23591274	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs13346221	chr19:23591275-23591276	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539827889	chr19:23591388-23591389	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs8109903	chr19:23591389-23591390	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11882651	chr19:23591396-23591397	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs187480954	chr19:23591397-23591398	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192196880	chr19:23591404-23591405	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150475574	chr19:23591428-23591429	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34916767	chr19:23591441-23591442	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs59310710	chr19:23591467-23591468	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548902063	chr19:23591470-23591471	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs8109710	chr19:23591474-23591475	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185038273	chr19:23591526-23591527	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368578880	chr19:23591527-23591528	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs8182600	chr19:23591537-23591538	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11880148	chr19:23591545-23591546	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs189092246	chr19:23591565-23591566	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560727185	chr19:23591583-23591584	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552310068	chr19:23591586-23591587	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570824835	chr19:23591602-23591603	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs199618257	chr19:23591615-23591616	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35257056	chr19:23591616-23591617	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs554806805	chr19:23591621-23591622	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201946064	chr19:23591623-23591624	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117495325	chr19:23591625-23591626	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs61417269	chr19:23591637-23591638	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:23578200-23598000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:23578400-23592200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:23578400-23597600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr19:23578600-23597800	Weak transcription	Fetal Stomach	stomach
5	chr19:23581600-23591000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr19:23581600-23591200	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr19:23581600-23591200	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr19:23581800-23591000	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr19:23582000-23594000	Enhancers	Fetal Intestine Large	intestine
10	chr19:23582200-23590800	Enhancers	Fetal Intestine Small	intestine
11	chr19:23582200-23591000	Strong transcription	H9 Cell Line	embryonic stem cell
12	chr19:23582600-23597600	Weak transcription	Fetal Brain Female	brain
13	chr19:23583800-23597600	Weak transcription	Fetal Lung	lung
14	chr19:23584400-23591800	Weak transcription	Small Intestine	intestine
15	chr19:23585400-23597400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr19:23585600-23597600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr19:23585800-23597800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr19:23586800-23597800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr19:23587000-23592400	Weak transcription	Colonic Mucosa	Colon
20	chr19:23587000-23598000	Weak transcription	Pancreas	Pancrea
21	chr19:23587200-23593000	Weak transcription	Stomach Mucosa	stomach
22	chr19:23587600-23598200	Weak transcription	Right Atrium	heart
23	chr19:23587800-23597600	Weak transcription	Brain Germinal Matrix	brain
24	chr19:23588000-23592400	Weak transcription	HepG2	liver
25	chr19:23588200-23597600	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr19:23589200-23591200	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr19:23589600-23591200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr19:23589800-23597400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr19:23590000-23591200	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr19:23590000-23596800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr19:23590200-23591200	Enhancers	Placenta	Placenta
32	chr19:23590200-23597400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr19:23590600-23590800	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
34	chr19:23590600-23591000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr19:23590600-23591000	Genic enhancers	Duodenum Mucosa	Duodenum
36	chr19:23590600-23591000	Genic enhancers	Rectal Mucosa Donor 31	rectum
37	chr19:23590600-23591200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr19:23590600-23591200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
39	chr19:23590800-23591200	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr19:23590800-23591800	Weak transcription	Fetal Intestine Small	intestine
41	chr19:23591000-23591800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr19:23591000-23591800	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr19:23591000-23597400	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr19:23591000-23597400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr19:23591000-23597400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr19:23591000-23597400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr19:23591200-23591600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr19:23591200-23591600	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr19:23591200-23592400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr19:23591200-23596800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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