Variant report

Variant	esv3323302
Chromosome Location	chr19:23477342-23648545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1866)
CpG islands
(count:612)
Chromatin interactive
region (count:16)
LncRNA
region (count:141)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1866 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:23586013-23586771	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:23582385-23582618	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:23584631-23584918	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:23592964-23593248	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:23577108-23577573	HepG2	liver:	n/a	n/a
6	ARID3A	chr19:23578021-23578544	HepG2	liver:	n/a	n/a
7	ATF1	chr19:23632171-23632277	K562	blood:	n/a	n/a
8	ATF1	chr19:23495315-23495375	K562	blood:	n/a	n/a
9	ATF1	chr19:23578242-23578507	K562	blood:	n/a	n/a
10	BACH1	chr19:23598347-23598392	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr19:23487075-23487353	K562	blood:	n/a	chr19:23487225-23487239
12	BACH1	chr19:23487080-23487334	H1-hESC	embryonic stem cell:	n/a	chr19:23487225-23487239
13	BCLAF1	chr19:23577806-23578259	GM12878	blood:	n/a	chr19:23577863-23577876
14	BCLAF1	chr19:23577695-23578386	GM12878	blood:	n/a	chr19:23577863-23577876
15	BHLHE40	chr19:23623769-23623831	HepG2	liver:	n/a	n/a
16	BHLHE40	chr19:23578060-23578466	GM12878	blood:	n/a	n/a
17	BRCA1	chr19:23577365-23578276	HepG2	liver:	n/a	n/a
18	BRCA1	chr19:23577422-23577533	GM12878	blood:	n/a	n/a
19	BRCA1	chr19:23577414-23577648	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr19:23598769-23598984	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr19:23577359-23578465	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr19:23493445-23494141	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr19:23490593-23491028	IMR90	lung:	n/a	n/a
24	CEBPB	chr19:23555128-23555243	IMR90	lung:	n/a	n/a
25	CEBPB	chr19:23500993-23501113	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:23590358-23590849	MCF-7	breast:	n/a	n/a
27	CEBPB	chr19:23641566-23642084	A549	lung:	n/a	chr19:23641688-23641699
28	CEBPB	chr19:23643455-23643717	HepG2	liver:	n/a	n/a
29	CEBPB	chr19:23504788-23505092	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr19:23578377-23578492	K562	blood:	n/a	n/a
31	CEBPB	chr19:23587676-23588015	HepG2	liver:	n/a	n/a
32	CEBPB	chr19:23589953-23590151	HepG2	liver:	n/a	n/a
33	CEBPB	chr19:23504745-23505381	HepG2	liver:	n/a	n/a
34	CEBPB	chr19:23578253-23578568	IMR90	lung:	n/a	n/a
35	CEBPB	chr19:23501811-23502717	A549	lung:	n/a	n/a
36	CEBPB	chr19:23526190-23526540	MCF-7	breast:	n/a	n/a
37	CEBPB	chr19:23644231-23644824	Hela-S3	cervix:	n/a	chr19:23644704-23644715
38	CEBPB	chr19:23646302-23646762	HepG2	liver:	n/a	n/a
39	CEBPB	chr19:23584727-23585585	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:23590437-23591084	IMR90	lung:	n/a	n/a
41	CEBPB	chr19:23578335-23578468	HepG2	liver:	n/a	n/a
42	CEBPB	chr19:23644084-23644837	A549	lung:	n/a	chr19:23644704-23644715
43	CEBPB	chr19:23590947-23591178	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr19:23583102-23583733	MCF-7	breast:	n/a	n/a
45	CEBPB	chr19:23503921-23504021	HepG2	liver:	n/a	n/a
46	CEBPB	chr19:23584688-23585615	A549	lung:	n/a	n/a
47	CEBPB	chr19:23641575-23642271	HepG2	liver:	n/a	chr19:23641688-23641699
48	CEBPB	chr19:23493473-23494015	IMR90	lung:	n/a	n/a
49	CEBPB	chr19:23575678-23575924	MCF-7	breast:	n/a	n/a
50	CEBPB	chr19:23574085-23574513	MCF-7	breast:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:23577714-23577764	HNPCEpiC	eye:	n/a
2	chr19:23578292-23578342	ProgFib	skin:	n/a
3	chr19:23577714-23577764	HNPCEpiC	eye:	n/a
4	chr19:23578292-23578342	ProgFib	skin:	n/a
5	chr19:23578679-23578729	HL-60	blood:	n/a
6	chr19:23578260-23578310	SK-N-SH_RA	brain:	n/a
7	chr19:23578292-23578342	AG10803	skin:	n/a
8	chr19:23577714-23577764	HCT-116	colon:	n/a
9	chr19:23578241-23578291	T-47D	breast:	n/a
10	chr19:23577714-23577764	NB4	blood:	n/a
11	chr19:23578679-23578729	NHDF-neo	bronchial:	n/a
12	chr19:23578292-23578342	BE2_C	brain:	n/a
13	chr19:23578260-23578310	HRCEpiC	kidney:	n/a
14	chr19:23578377-23578427	HMEC	breast:	n/a
15	chr19:23578063-23578113	AG09319	gingival:	n/a
16	chr19:23578063-23578113	Caco-2	colon:	n/a
17	chr19:23578365-23578415	K562	blood:	n/a
18	chr19:23578679-23578729	SAEC	small airway:	n/a
19	chr19:23578292-23578342	NT2-D1	testis:	n/a
20	chr19:23541643-23541693	RPTEC	kidney:	n/a
21	chr19:23577714-23577764	Jurkat	blood:	n/a
22	chr19:23578260-23578310	A549	lung:	n/a
23	chr19:23578377-23578427	HCPEpiC	choroid plexus:	n/a
24	chr19:23598854-23598904	H1-hESC	embryonic stem cell:	embryo
25	chr19:23578292-23578342	HAEpiC	amniotic membrane:	n/a
26	chr19:23578241-23578291	HUVEC	blood vessel:	n/a
27	chr19:23578241-23578291	H1-hESC	embryonic stem cell:	embryo
28	chr19:23577714-23577764	HRCEpiC	kidney:	n/a
29	chr19:23541643-23541693	MCF10A-Er-Src	breast:	n/a
30	chr19:23578365-23578415	U87	brain:	n/a
31	chr19:23577714-23577764	SK-N-MC	brain:	n/a
32	chr19:23578377-23578427	HCM	heart:	n/a
33	chr19:23578063-23578113	SAEC	small airway:	n/a
34	chr19:23598854-23598904	NH-A	brain:	n/a
35	chr19:23578292-23578342	HIPEpiC	eye:	n/a
36	chr19:23578260-23578310	AG09319	gingival:	n/a
37	chr19:23578241-23578291	HCF	heart:	n/a
38	chr19:23578365-23578415	MCF-7	breast:	n/a
39	chr19:23577714-23577764	AG10803	skin:	n/a
40	chr19:23578063-23578113	PrEC	prostate:	n/a
41	chr19:23577714-23577764	HUVEC	blood vessel:	n/a
42	chr19:23578365-23578415	BE2_C	brain:	n/a
43	chr19:23578377-23578427	SKMC	muscle:	n/a
44	chr19:23578063-23578113	LNCaP	prostate:	n/a
45	chr19:23577714-23577764	AG09309	skin:	n/a
46	chr19:23577714-23577764	PFSK-1	brain:	n/a
47	chr19:23578063-23578113	Hepatocyte	liver:	n/a
48	chr19:23578260-23578310	ECC-1	luminal epithelium:	n/a
49	chr19:23578292-23578342	HCT-116	colon:	n/a
50	chr19:23541643-23541693	GM12892	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:23564648..23566828-chr19:23577196..23579466,2	MCF-7	breast:
2	chr19:23574385..23576315-chr19:23576535..23579430,2	K562	blood:
3	chr19:23571146..23573840-chr19:23574386..23577614,3	K562	blood:
4	chr19:23571146..23574036-chr19:23574733..23577243,2	K562	blood:
5	chr19:23571146..23573840-chr19:23574386..23577614,3	K562	blood:
6	chr19:23571146..23574036-chr19:23574733..23577243,2	K562	blood:
7	chr19:23598116..23599107-chr19:24216116..24216947,3	MCF-7	breast:
8	chr19:23576348..23579660-chr19:23867719..23870587,3	MCF-7	breast:
9	chr19:23598106..23598617-chr19:24216264..24217103,2	MCF-7	breast:
10	chr19:23520093..23520713-chr21:9826403..9827051,2	MCF-7	breast:
11	chr19:23597107..23600085-chr19:24215651..24217575,2	MCF-7	breast:
12	chr19:23597097..23600084-chr19:24215418..24217838,2	MCF-7	breast:
13	chr19:23576617..23579164-chr19:23594549..23597394,2	MCF-7	breast:
14	chr19:23577154..23579229-chr19:23583278..23584951,2	MCF-7	breast:
15	chr19:23598051..23598951-chr19:24216258..24216783,2	NB4	blood:
16	chr19:23577656..23578478-chr19:49121947..49122666,2	NB4	blood:

(count:141 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF91-1	chr19:23586008-23586295	ENSG00000269416.1
2	lnc-ZNF91-1	chr19:23588802-23588899	NONHSAT063917
3	lnc-AC092329.1-2	chr19:23493350-23493504	XLOC_013275
4	lnc-AC092329.1-2	chr19:23487801-23487933	NONHSAT063886
5	lnc-ZNF91-1	chr19:23598706-23598876	ENSG00000269416.1
6	lnc-AC092329.1-2	chr19:23490106-23490204	NONHSAT063893
7	lnc-AC092329.1-2	chr19:23500843-23500875	NONHSAT063885
8	lnc-ZNF91-1	chr19:23586008-23586311	ENSG00000269416.1
9	lnc-ZNF91-1	chr19:23582038-23583849	NONHSAT063908
10	lnc-ZNF91-1	chr19:23587753-23587910	ENSG00000269416.1
11	lnc-AC092329.1-2	chr19:23522033-23522062	NONHSAT063902
12	lnc-ZNF730-16	chr19:23627064-23627991	NONHSAT063920
13	lnc-ZNF91-1	chr19:23586522-23586549	ENSG00000269416.1
14	lnc-AC092329.1-2	chr19:23497078-23497228	NONHSAT063885
15	lnc-ZNF730-14	chr19:23586491-23586538	NONHSAT063915
16	lnc-AC092329.1-2	chr19:23487809-23487933	XLOC_013275
17	lnc-ZNF91-1	chr19:23586522-23586549	NONHSAT063908
18	lnc-ZNF91-1	chr19:23588802-23588899	NONHSAT063918
19	lnc-ZNF91-1	chr19:23586008-23586295	NONHSAT063908
20	lnc-ZNF91-1	chr19:23588060-23588137	ENSG00000269416.1
21	lnc-AC092329.1-2	chr19:23493124-23493230	XLOC_013275
22	lnc-ZNF91-1	chr19:23585219-23585314	ENSG00000269416.1
23	lnc-ZNF91-1	chr19:23588060-23588137	ENSG00000269416.1
24	lnc-ZNF91-1	chr19:23582035-23583849	ENSG00000269416.1
25	lnc-ZNF91-1	chr19:23582272-23583849	ENSG00000269416.1
26	lnc-ZNF91-1	chr19:23588060-23588137	ENSG00000269416.1
27	lnc-AC092329.1-2	chr19:23491726-23491899	XLOC_013275
28	lnc-ZNF91-1	chr19:23598696-23598867	ENSG00000269416.1
29	lnc-ZNF91-1	chr19:23587726-23587910	NONHSAT063918
30	lnc-ZNF91-1	chr19:23598696-23598849	ENSG00000269416.1
31	lnc-AC092329.1-2	chr19:23541232-23541650	NONHSAT063902
32	lnc-ZNF91-1	chr19:23588060-23588137	ENSG00000246181
33	lnc-AC092329.1-2	chr19:23493350-23493434	XLOC_013275
34	lnc-ZNF91-1	chr19:23598706-23598867	ENSG00000269416.1
35	lnc-AC092329.1-2	chr19:23524972-23525067	NONHSAT063902
36	lnc-ZNF91-1	chr19:23586008-23586295	ENSG00000246181
37	lnc-ZNF91-1	chr19:23587753-23587910	ENSG00000269416.1
38	lnc-ZNF91-1	chr19:23584979-23585314	ENSG00000269416.1
39	lnc-ZNF91-1	chr19:23598696-23598903	NONHSAT063906
40	lnc-ZNF91-1	chr19:23586522-23586549	ENSG00000246181
41	lnc-ZNF91-1	chr19:23586008-23586312	NONHSAT063911
42	lnc-ZNF91-1	chr19:23598706-23598876	ENSG00000269416.1
43	lnc-ZNF91-1	chr19:23586008-23586311	ENSG00000269416.1
44	lnc-AC092329.1-2	chr19:23493124-23493230	XLOC_013275
45	lnc-AC092329.1-2	chr19:23521418-23521856	NONHSAT063901
46	lnc-ZNF91-1	chr19:23586522-23586549	ENSG00000246181
47	lnc-ZNF91-1	chr19:23583789-23583849	ENSG00000269416.1
48	lnc-ZNF91-1	chr19:23587753-23587910	NONHSAT063917
49	lnc-ZNF91-1	chr19:23590700-23590900	NONHSAT063908
50	lnc-AC092329.1-2	chr19:23490118-23490204	NONHSAT063886

No data

Variant related genes	Relation type
ENSG00000269416	TF binding region
ENSG00000268992	TF binding region
ENSG00000269431	TF binding region
VN1R92P	TF binding region
ZNF91	TF binding region
ENSG00000267934	TF binding region
ENSG00000269416	CpG island
ENSG00000268992	CpG island
ENSG00000269431	CpG island
VN1R92P	CpG island
ZNF91	CpG island
ENSG00000267934	CpG island
ENSG00000213096	chromatin interactions
ENSG00000063177	chromatin interactions
ENSG00000197372	chromatin interactions
ENSG00000167232	chromatin interactions
ENSG00000268362	chromatin interactions
ENSG00000063176	chromatin interactions
EIF2C2	miRNA target sites
NR3C2	miRNA target sites
FAM199X	miRNA target sites
DNMBP	miRNA target sites
EIF1AX	miRNA target sites
TNKS	miRNA target sites
TES	miRNA target sites
HIATL1	miRNA target sites
ELMO2	miRNA target sites
SP4	miRNA target sites
ALG9	miRNA target sites
NR4A1	miRNA target sites
ELK4	miRNA target sites
ELK3	miRNA target sites
GABRB3	miRNA target sites
SOD2	miRNA target sites
TBC1D22B	miRNA target sites
ARF3	miRNA target sites
ARCN1	miRNA target sites
TMEM30A	miRNA target sites
PLS3	miRNA target sites
GTF2IRD2	miRNA target sites
NFIB	miRNA target sites

Extended variants
information (count: 5533 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:5533 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79351099	chr19:23477350-23477351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73016386	chr19:23477367-23477368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368438339	chr19:23477387-23477388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186186805	chr19:23477389-23477390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200372505	chr19:23477404-23477405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201528693	chr19:23477409-23477410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149099600	chr19:23477417-23477418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73563444	chr19:23477428-23477429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112036794	chr19:23477458-23477459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201752270	chr19:23477465-23477466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200563437	chr19:23477485-23477486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76301699	chr19:23477488-23477489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562514577	chr19:23477513-23477514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570674937	chr19:23477517-23477518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76278741	chr19:23477540-23477541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78778054	chr19:23477550-23477551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530017253	chr19:23477561-23477562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75173502	chr19:23477568-23477569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74369117	chr19:23477585-23477586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79472844	chr19:23477602-23477603	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs73016388	chr19:23477603-23477604	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs190883324	chr19:23477610-23477611	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs201117205	chr19:23477619-23477620	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs531279307	chr19:23477630-23477631	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs75898154	chr19:23477634-23477635	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs79336435	chr19:23477639-23477640	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs12610450	chr19:23477645-23477646	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs143137144	chr19:23477646-23477647	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs12610467	chr19:23477648-23477649	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs12610446	chr19:23477666-23477667	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs566364977	chr19:23477680-23477681	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs12610458	chr19:23477681-23477682	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs12610449	chr19:23477686-23477687	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs567417794	chr19:23477712-23477713	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs167153	chr19:23477713-23477714	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs180979689	chr19:23477729-23477730	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs34842987	chr19:23477738-23477739	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs555814661	chr19:23477749-23477750	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs77470723	chr19:23477757-23477758	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs76849165	chr19:23477764-23477765	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs73563447	chr19:23477790-23477791	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs375554108	chr19:23477819-23477820	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs574573814	chr19:23477821-23477822	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs73563449	chr19:23477851-23477852	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs73563453	chr19:23477914-23477915	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs535536652	chr19:23477936-23477937	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs375967789	chr19:23477937-23477938	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs169798	chr19:23477948-23477949	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs150318382	chr19:23477957-23477958	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs34920996	chr19:23477983-23477984	Weak transcription Active TSS	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3371 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:23468600-23492600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr19:23477600-23478000	Active TSS	Brain Substantia Nigra	brain
3	chr19:23485200-23486400	ZNF genes & repeats	Dnd41	blood
4	chr19:23486200-23490000	Weak transcription	Placenta	Placenta
5	chr19:23486400-23486800	Flanking Active TSS	Dnd41	blood
6	chr19:23486400-23508000	Weak transcription	Ovary	ovary
7	chr19:23488200-23489800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr19:23488200-23490000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr19:23488600-23491000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr19:23488800-23490400	Weak transcription	Left Ventricle	heart
11	chr19:23489200-23491200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr19:23489400-23492800	Weak transcription	Fetal Muscle Trunk	muscle
13	chr19:23489800-23490400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
14	chr19:23489800-23492400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr19:23489800-23498200	Weak transcription	Aorta	Aorta
16	chr19:23490000-23491800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr19:23490000-23491800	Strong transcription	Placenta	Placenta
18	chr19:23490000-23493400	Weak transcription	Brain Anterior Caudate	brain
19	chr19:23490000-23514200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr19:23490200-23491600	ZNF genes & repeats	Fetal Brain Female	brain
21	chr19:23490400-23491400	Strong transcription	Pancreatic Islets	Pancreatic Islet
22	chr19:23490400-23491800	Strong transcription	Left Ventricle	heart
23	chr19:23490400-23500800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr19:23490600-23491800	ZNF genes & repeats	Brain Germinal Matrix	brain
25	chr19:23491000-23491800	Strong transcription	Skeletal Muscle Female	skeletal muscle
26	chr19:23491200-23492000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr19:23491400-23493200	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr19:23491800-23493400	Weak transcription	Placenta	Placenta
29	chr19:23491800-23493400	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr19:23491800-23508400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr19:23491800-23512800	Weak transcription	Left Ventricle	heart
32	chr19:23492000-23493600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr19:23492400-23502600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr19:23492600-23493600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr19:23493400-23499800	Enhancers	Placenta	Placenta
36	chr19:23493600-23494800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr19:23494200-23494400	Enhancers	Placenta Amnion	Placenta Amnion
38	chr19:23494400-23518200	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr19:23494800-23496600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr19:23496600-23512200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr19:23496800-23498400	ZNF genes & repeats	Fetal Brain Female	brain
42	chr19:23499800-23500800	Weak transcription	Placenta	Placenta
43	chr19:23500400-23516600	Weak transcription	Right Ventricle	heart
44	chr19:23500800-23501000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
45	chr19:23500800-23505800	Enhancers	Placenta	Placenta
46	chr19:23501000-23501800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr19:23501200-23512600	Weak transcription	Brain Cingulate Gyrus	brain
48	chr19:23502600-23503000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr19:23503000-23503400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr19:23504200-23507800	Weak transcription	Aorta	Aorta

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