Variant report

Variant	nsv1060072
Chromosome Location	chr19:56289331-56450495
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:1771)
Chromatin interactive
region (count:23)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr19:56320795-56321061	K562	blood:	n/a	n/a
2	ATF3	chr19:56320785-56321060	GM12878	blood:	n/a	n/a
3	BATF	chr19:56404597-56404754	GM12878	blood:	n/a	n/a
4	BCL11A	chr19:56404601-56404738	GM12878	blood:	n/a	n/a
5	BCL11A	chr19:56404582-56404766	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:56320723-56321185	K562	blood:	n/a	n/a
7	BHLHE40	chr19:56320784-56321089	HepG2	liver:	n/a	n/a
8	CBX3	chr19:56320742-56321100	K562	blood:	n/a	n/a
9	CBX3	chr19:56320575-56321158	K562	blood:	n/a	n/a
10	CBX3	chr19:56347744-56348093	K562	blood:	n/a	n/a
11	CEBPB	chr19:56303064-56303264	K562	blood:	n/a	chr19:56303175-56303186 chr19:56303172-56303189
12	CEBPB	chr19:56341872-56342423	HCT-116	colon:	n/a	n/a
13	CEBPB	chr19:56313719-56313987	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr19:56306047-56306327	HepG2	liver:	n/a	chr19:56306161-56306174 chr19:56306161-56306172
15	CEBPB	chr19:56303142-56303233	A549	lung:	n/a	chr19:56303175-56303186 chr19:56303172-56303189
16	CEBPB	chr19:56306160-56306187	Hela-S3	cervix:	n/a	chr19:56306161-56306174 chr19:56306161-56306172
17	CEBPB	chr19:56406673-56406772	HepG2	liver:	n/a	chr19:56406697-56406708
18	CEBPB	chr19:56448024-56448130	K562	blood:	n/a	n/a
19	CEBPB	chr19:56342078-56342348	HepG2	liver:	n/a	n/a
20	CEBPB	chr19:56448047-56448229	IMR90	lung:	n/a	n/a
21	CEBPB	chr19:56342114-56342249	K562	blood:	n/a	n/a
22	CEBPB	chr19:56448063-56448170	A549	lung:	n/a	n/a
23	CEBPB	chr19:56344099-56344348	A549	lung:	n/a	n/a
24	CEBPB	chr19:56320804-56321149	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr19:56309941-56309963	HepG2	liver:	n/a	chr19:56309945-56309956
26	CEBPB	chr19:56342021-56342353	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr19:56413999-56414214	HepG2	liver:	n/a	chr19:56414104-56414121 chr19:56414107-56414118 chr19:56414109-56414120 chr19:56414107-56414120 chr19:56414107-56414120
28	CEBPB	chr19:56341826-56342415	HCT-116	colon:	n/a	n/a
29	CEBPB	chr19:56342129-56342342	K562	blood:	n/a	n/a
30	CEBPB	chr19:56448058-56448093	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr19:56384985-56385182	HepG2	liver:	n/a	n/a
32	CEBPB	chr19:56385000-56385192	K562	blood:	n/a	n/a
33	CEBPB	chr19:56303101-56303314	HepG2	liver:	n/a	chr19:56303175-56303186 chr19:56303172-56303189
34	CEBPB	chr19:56413977-56414273	K562	blood:	n/a	chr19:56414104-56414121 chr19:56414107-56414118 chr19:56414109-56414120 chr19:56414107-56414120 chr19:56414107-56414120
35	CREB1	chr19:56368555-56368853	GM12878	blood:	n/a	n/a
36	CREB1	chr19:56410261-56410516	A549	lung:	n/a	n/a
37	CREB1	chr19:56320773-56321071	A549	lung:	n/a	n/a
38	CTCF	chr19:56425140-56425290	GM12869	blood:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
39	CTCF	chr19:56320980-56321130	BJ	skin:	n/a	n/a
40	CTCF	chr19:56425146-56425355	SK-N-SH_RA	brain:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
41	CTCF	chr19:56425160-56425310	GM12873	blood:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
42	CTCF	chr19:56425285-56425295	GM20000	blood:	n/a	n/a
43	CTCF	chr19:56425158-56425328	H1-hESC	embryonic stem cell:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
44	CTCF	chr19:56321140-56321290	Caco-2	colon:	n/a	n/a
45	CTCF	chr19:56320881-56321100	A549	lung:	n/a	n/a
46	CTCF	chr19:56425260-56425410	GM12872	blood:	n/a	n/a
47	CTCF	chr19:56425140-56425290	SAEC	small airway:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
48	CTCF	chr19:56425120-56425270	GM12871	blood:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
49	CTCF	chr19:56320960-56321110	HMEC	breast:	n/a	n/a
50	CTCF	chr19:56425200-56425350	GM12864	blood:	n/a	chr19:56425239-56425257 chr19:56425242-56425255

(count:1771 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56348889-56348939	NHDF-neo	bronchial:	n/a
2	chr19:56347927-56347977	IMR90	lung:	fetal
3	chr19:56348889-56348939	NHDF-neo	bronchial:	n/a
4	chr19:56347927-56347977	IMR90	lung:	fetal
5	chr19:56347870-56347920	HEEpiC	esophagus:	n/a
6	chr19:56369928-56369978	LNCaP	prostate:	n/a
7	chr19:56367316-56367366	AG09319	gingival:	n/a
8	chr19:56444551-56444601	AG04449	skin:	fetal
9	chr19:56443419-56443469	AoSMC	blood vessel:	n/a
10	chr19:56346743-56346793	AG10803	skin:	n/a
11	chr19:56364183-56364233	AG10803	skin:	n/a
12	chr19:56443419-56443469	BE2_C	brain:	n/a
13	chr19:56369522-56369572	U87	brain:	n/a
14	chr19:56369522-56369572	NHDF-neo	bronchial:	n/a
15	chr19:56348742-56348792	HRE	kidney:	n/a
16	chr19:56369522-56369572	AG04449	skin:	fetal
17	chr19:56346628-56346678	SK-N-SH	brain:	n/a
18	chr19:56348742-56348792	HCPEpiC	choroid plexus:	n/a
19	chr19:56361716-56361766	U87	brain:	n/a
20	chr19:56369602-56369652	Hela-S3	cervix:	n/a
21	chr19:56347847-56347897	MCF10A-Er-Src	breast:	n/a
22	chr19:56347927-56347977	HRPEpiC	eye:	n/a
23	chr19:56366191-56366241	HCT-116	colon:	n/a
24	chr19:56348742-56348792	H1-hESC	embryonic stem cell:	embryo
25	chr19:56349119-56349169	SK-N-MC	brain:	n/a
26	chr19:56349119-56349169	AoSMC	blood vessel:	n/a
27	chr19:56348742-56348792	HEK293	kidney:	embryo
28	chr19:56347847-56347897	ProgFib	skin:	n/a
29	chr19:56321115-56321165	SAEC	small airway:	n/a
30	chr19:56321115-56321165	AG10803	skin:	n/a
31	chr19:56364183-56364233	NT2-D1	testis:	n/a
32	chr19:56347847-56347897	GM12891	blood:	n/a
33	chr19:56369416-56369466	SK-N-SH_RA	brain:	n/a
34	chr19:56346743-56346793	SK-N-SH	brain:	n/a
35	chr19:56348889-56348939	PANC-1	pancreas:	n/a
36	chr19:56346743-56346793	H1-hESC	embryonic stem cell:	embryo
37	chr19:56361716-56361766	PrEC	prostate:	n/a
38	chr19:56444163-56444213	H1-hESC	embryonic stem cell:	embryo
39	chr19:56348889-56348939	HEEpiC	esophagus:	n/a
40	chr19:56443419-56443469	Hepatocyte	liver:	n/a
41	chr19:56342665-56342715	HepG2	liver:	n/a
42	chr19:56348742-56348792	RPTEC	kidney:	n/a
43	chr19:56444163-56444213	AG09319	gingival:	n/a
44	chr19:56348216-56348266	HRE	kidney:	n/a
45	chr19:56367830-56367880	HRPEpiC	eye:	n/a
46	chr19:56347771-56347821	HEK293	kidney:	embryo
47	chr19:56348216-56348266	Hepatocyte	liver:	n/a
48	chr19:56321115-56321165	HPAEpiC	pulmonary alveolar:	n/a
49	chr19:56348889-56348939	T-47D	breast:	n/a
50	chr19:56348216-56348266	IMR90	lung:	fetal

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:56154646..56157469-chr19:56320244..56322064,2	K562	blood:
2	chr19:56373661..56375169-chr19:56376696..56378685,2	K562	blood:
3	chr19:56424869..56425718-chr19:56582163..56583125,2	MCF-7	breast:
4	chr19:56321292..56324216-chr19:56328648..56330959,2	K562	blood:
5	chr19:56288962..56289563-chr19:56320651..56321410,3	MCF-7	breast:
6	chr19:56373661..56375169-chr19:56376696..56378685,2	K562	blood:
7	chr19:56164701..56165323-chr19:56320540..56321426,2	MCF-7	breast:
8	chr19:56294175..56296046-chr19:56307232..56309273,2	MCF-7	breast:
9	chr19:56439351..56441429-chr19:56446067..56448328,2	MCF-7	breast:
10	chr19:56430402..56432379-chr19:56447676..56449907,2	K562	blood:
11	chr19:56143497..56144412-chr19:56320540..56321434,5	K562	blood:
12	chr19:56311206..56314019-chr19:56318458..56321376,2	K562	blood:
13	chr19:56327095..56328748-chr19:56329446..56331884,2	K562	blood:
14	chr19:56439351..56441429-chr19:56446067..56448328,2	MCF-7	breast:
15	chr19:56288962..56289563-chr19:56320651..56321410,3	MCF-7	breast:
16	chr19:56320256..56321150-chr19:56577550..56578288,2	K562	blood:
17	chr19:56437345..56439386-chr19:56452694..56454259,2	K562	blood:
18	chr19:56311206..56314019-chr19:56318458..56321376,2	K562	blood:
19	chr19:56294175..56296046-chr19:56307232..56309273,2	MCF-7	breast:
20	chr17:41464575..41466240-chr19:56288867..56290367,2	K562	blood:
21	chr19:56015535..56016051-chr19:56320998..56321733,2	K562	blood:
22	chr19:56430402..56432379-chr19:56447676..56449907,2	K562	blood:
23	chr19:56230205..56232527-chr19:56319829..56322446,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NLRP4-1	chr19:56399226-56399347	XLOC_013162
2	lnc-NLRP4-1	chr19:56400283-56401109	XLOC_013162

No data

Variant related genes	Relation type
NLRP13	TF binding region
NLRP11	TF binding region
NLRP4	TF binding region
NLRP13	CpG island
NLRP11	CpG island
NLRP4	CpG island
ENSG00000171425	chromatin interactions
ENSG00000267522	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000179873	chromatin interactions

Extended variants
information (count: 2766 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2766 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577489165	chr19:56289358-56289359	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs540090783	chr19:56289380-56289381	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs556291078	chr19:56289382-56289383	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs532503499	chr19:56289404-56289405	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs113153110	chr19:56289444-56289445	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs541816469	chr19:56289452-56289453	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555479387	chr19:56289521-56289522	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572189560	chr19:56289561-56289562	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs188991154	chr19:56289567-56289568	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373303171	chr19:56289581-56289582	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs181708947	chr19:56289582-56289583	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs187356855	chr19:56289603-56289604	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs560263340	chr19:56289607-56289608	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs532316859	chr19:56289678-56289679	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552465460	chr19:56289695-56289696	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546034513	chr19:56289697-56289698	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs562639865	chr19:56289719-56289720	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs192119851	chr19:56289723-56289724	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562755451	chr19:56289755-56289756	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs150435382	chr19:56289769-56289770	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568190471	chr19:56289797-56289798	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs182405873	chr19:56289836-56289837	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs527353153	chr19:56289857-56289858	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547688849	chr19:56289895-56289896	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185787340	chr19:56289916-56289917	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs539745976	chr19:56289927-56289928	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375394313	chr19:56289943-56289944	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs570003868	chr19:56289953-56289954	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs371513507	chr19:56289965-56289966	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs117303094	chr19:56289969-56289970	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs61745325	chr19:56290078-56290079	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs189771544	chr19:56290140-56290141	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541476729	chr19:56290169-56290170	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs8112672	chr19:56290178-56290179	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs577016475	chr19:56290193-56290194	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545671854	chr19:56290208-56290209	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs148885980	chr19:56290223-56290224	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs61740704	chr19:56290237-56290238	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs182427445	chr19:56290289-56290290	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs8112907	chr19:56290361-56290362	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs143009950	chr19:56293202-56293203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544773565	chr19:56293234-56293235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188059238	chr19:56293248-56293249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538888022	chr19:56293277-56293278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539472621	chr19:56293289-56293290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559077843	chr19:56293290-56293291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371316025	chr19:56293291-56293292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576021610	chr19:56293295-56293296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544875421	chr19:56293296-56293297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561267170	chr19:56293320-56293321	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
Breast cancer	21509527	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20409316	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56293200-56293400	Enhancers	Hela-S3	cervix
2	chr19:56295400-56295600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
3	chr19:56300600-56304000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr19:56306200-56310800	Weak transcription	Pancreas	Pancrea
5	chr19:56307400-56313400	Weak transcription	Liver	Liver
6	chr19:56312000-56313000	Enhancers	GM12878-XiMat	blood
7	chr19:56312800-56313200	Active TSS	Brain Substantia Nigra	brain
8	chr19:56312800-56313400	Enhancers	Primary B cells from peripheral blood	blood
9	chr19:56313000-56313400	Flanking Active TSS	GM12878-XiMat	blood
10	chr19:56313000-56313400	Enhancers	Hela-S3	cervix
11	chr19:56313200-56315600	Weak transcription	Brain Substantia Nigra	brain
12	chr19:56313400-56314200	Enhancers	Liver	Liver
13	chr19:56313800-56314000	Enhancers	Hela-S3	cervix
14	chr19:56315600-56316000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr19:56315600-56316200	ZNF genes & repeats	Brain Substantia Nigra	brain
16	chr19:56316200-56320800	Weak transcription	Brain Substantia Nigra	brain
17	chr19:56318800-56319800	Weak transcription	Liver	Liver
18	chr19:56319800-56320600	Enhancers	Liver	Liver
19	chr19:56320200-56321000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
20	chr19:56320400-56320600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr19:56320400-56321000	ZNF genes & repeats	A549	lung
22	chr19:56320400-56321200	Enhancers	GM12878-XiMat	blood
23	chr19:56320600-56320800	Active TSS	Adipose Nuclei	Adipose
24	chr19:56320600-56320800	Flanking Active TSS	Hela-S3	cervix
25	chr19:56320600-56321000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr19:56320600-56321000	Flanking Active TSS	Liver	Liver
27	chr19:56320600-56321000	Active TSS	Duodenum Mucosa	Duodenum
28	chr19:56320600-56321000	Enhancers	Pancreas	Pancrea
29	chr19:56320600-56321000	Active TSS	Rectal Mucosa Donor 29	rectum
30	chr19:56320600-56321000	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr19:56320600-56321000	Flanking Active TSS	K562	blood
32	chr19:56320600-56321400	Enhancers	Primary B cells from peripheral blood	blood
33	chr19:56320800-56321000	Flanking Active TSS	Adipose Nuclei	Adipose
34	chr19:56320800-56321000	ZNF genes & repeats	Fetal Intestine Small	intestine
35	chr19:56320800-56321000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
36	chr19:56320800-56321200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr19:56320800-56321200	Bivalent Enhancer	Brain Anterior Caudate	brain
38	chr19:56320800-56321200	Active TSS	Hela-S3	cervix
39	chr19:56320800-56321400	Active TSS	Brain Substantia Nigra	brain
40	chr19:56321000-56321400	Enhancers	Liver	Liver
41	chr19:56321000-56321400	Enhancers	K562	blood
42	chr19:56321000-56323000	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr19:56321200-56321400	Flanking Active TSS	Hela-S3	cervix
44	chr19:56329400-56330200	Enhancers	GM12878-XiMat	blood
45	chr19:56329600-56334200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
46	chr19:56330200-56331800	Flanking Active TSS	GM12878-XiMat	blood
47	chr19:56330200-56332000	Enhancers	Primary B cells from peripheral blood	blood
48	chr19:56331200-56331800	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr19:56331800-56332600	Enhancers	GM12878-XiMat	blood
50	chr19:56333400-56334000	Active TSS	ES-I3 Cell Line	embryonic stem cell

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