Variant report

Variant	nsv1064105
Chromosome Location	chr19:56319416-56450532
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:615)
CpG islands
(count:1770)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:615 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr19:56320784-56321089	HepG2	liver:	n/a	n/a
7	BHLHE40	chr19:56320723-56321185	K562	blood:	n/a	n/a
8	CBX3	chr19:56347744-56348093	K562	blood:	n/a	n/a
9	CBX3	chr19:56320742-56321100	K562	blood:	n/a	n/a
10	CBX3	chr19:56320575-56321158	K562	blood:	n/a	n/a
11	CEBPB	chr19:56384985-56385182	HepG2	liver:	n/a	n/a
12	CEBPB	chr19:56341826-56342415	HCT-116	colon:	n/a	n/a
13	CEBPB	chr19:56320804-56321149	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr19:56448063-56448170	A549	lung:	n/a	n/a
15	CEBPB	chr19:56413977-56414273	K562	blood:	n/a	chr19:56414104-56414121 chr19:56414107-56414118 chr19:56414109-56414120 chr19:56414107-56414120 chr19:56414107-56414120
16	CEBPB	chr19:56342114-56342249	K562	blood:	n/a	n/a
17	CEBPB	chr19:56342021-56342353	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr19:56448047-56448229	IMR90	lung:	n/a	n/a
19	CEBPB	chr19:56448058-56448093	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr19:56342129-56342342	K562	blood:	n/a	n/a
21	CEBPB	chr19:56406673-56406772	HepG2	liver:	n/a	chr19:56406697-56406708
22	CEBPB	chr19:56448024-56448130	K562	blood:	n/a	n/a
23	CEBPB	chr19:56413999-56414214	HepG2	liver:	n/a	chr19:56414104-56414121 chr19:56414107-56414118 chr19:56414109-56414120 chr19:56414107-56414120 chr19:56414107-56414120
24	CEBPB	chr19:56385000-56385192	K562	blood:	n/a	n/a
25	CEBPB	chr19:56341872-56342423	HCT-116	colon:	n/a	n/a
26	CEBPB	chr19:56342078-56342348	HepG2	liver:	n/a	n/a
27	CEBPB	chr19:56344099-56344348	A549	lung:	n/a	n/a
28	CREB1	chr19:56410261-56410516	A549	lung:	n/a	n/a
29	CREB1	chr19:56320773-56321071	A549	lung:	n/a	n/a
30	CREB1	chr19:56368555-56368853	GM12878	blood:	n/a	n/a
31	CTCF	chr19:56425160-56425310	SK-N-SH_RA	brain:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
32	CTCF	chr19:56320960-56321110	GM12867	blood:	n/a	n/a
33	CTCF	chr19:56320940-56321090	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr19:56425176-56425314	Kidney_OC	kidney:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
35	CTCF	chr19:56425180-56425330	K562	blood:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
36	CTCF	chr19:56320764-56321191	HepG2	liver:	n/a	n/a
37	CTCF	chr19:56425180-56425330	HRE	kidney:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
38	CTCF	chr19:56425071-56425360	K562	blood:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
39	CTCF	chr19:56320753-56320782	LNCaP	prostate:	n/a	n/a
40	CTCF	chr19:56425220-56425370	GM12869	blood:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
41	CTCF	chr19:56425160-56425310	GM12864	blood:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
42	CTCF	chr19:56321020-56321170	GM12872	blood:	n/a	n/a
43	CTCF	chr19:56425260-56425410	GM12872	blood:	n/a	n/a
44	CTCF	chr19:56320960-56321110	GM12875	blood:	n/a	n/a
45	CTCF	chr19:56320757-56321144	K562	blood:	n/a	n/a
46	CTCF	chr19:56425124-56425365	MCF-7	breast:	n/a	chr19:56425239-56425257 chr19:56425242-56425255
47	CTCF	chr19:56320960-56321110	HMEC	breast:	n/a	n/a
48	CTCF	chr19:56320862-56321115	A549	lung:	n/a	n/a
49	CTCF	chr19:56320940-56321090	HRE	kidney:	n/a	n/a
50	CTCF	chr19:56320920-56321070	HPAF	blood vessel:	n/a	n/a

(count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56347771-56347821	HEEpiC	esophagus:	n/a
2	chr19:56347771-56347821	HEEpiC	esophagus:	n/a
3	chr19:56444163-56444213	SK-N-SH	brain:	n/a
4	chr19:56369928-56369978	HRE	kidney:	n/a
5	chr19:56348216-56348266	GM19239	blood:	n/a
6	chr19:56361716-56361766	RPTEC	kidney:	n/a
7	chr19:56418660-56418710	AG04449	skin:	fetal
8	chr19:56348889-56348939	K562	blood:	n/a
9	chr19:56393163-56393213	HCPEpiC	choroid plexus:	n/a
10	chr19:56393163-56393213	SKMC	muscle:	n/a
11	chr19:56321115-56321165	HCT-116	colon:	n/a
12	chr19:56443419-56443469	GM12892	blood:	n/a
13	chr19:56444163-56444213	PANC-1	pancreas:	n/a
14	chr19:56363105-56363155	SK-N-SH_RA	brain:	n/a
15	chr19:56366191-56366241	MCF10A-Er-Src	breast:	n/a
16	chr19:56347927-56347977	MCF-7	breast:	n/a
17	chr19:56367316-56367366	NT2-D1	testis:	n/a
18	chr19:56342665-56342715	NH-A	brain:	n/a
19	chr19:56349119-56349169	BE2_C	brain:	n/a
20	chr19:56366191-56366241	GM12878	blood:	n/a
21	chr19:56367830-56367880	CMK	blood:	n/a
22	chr19:56418660-56418710	A549	lung:	n/a
23	chr19:56347927-56347977	HL-60	blood:	n/a
24	chr19:56367316-56367366	CMK	blood:	n/a
25	chr19:56347771-56347821	HCT-116	colon:	n/a
26	chr19:56342665-56342715	HPAEpiC	pulmonary alveolar:	n/a
27	chr19:56349119-56349169	LNCaP	prostate:	n/a
28	chr19:56347722-56347772	NHDF-neo	bronchial:	n/a
29	chr19:56393163-56393213	NB4	blood:	n/a
30	chr19:56367316-56367366	HNPCEpiC	eye:	n/a
31	chr19:56347847-56347897	AG04449	skin:	fetal
32	chr19:56321115-56321165	H1-hESC	embryonic stem cell:	embryo
33	chr19:56347927-56347977	NHDF-neo	bronchial:	n/a
34	chr19:56444551-56444601	HCM	heart:	n/a
35	chr19:56369416-56369466	BJ	skin:	n/a
36	chr19:56342665-56342715	HepG2	liver:	n/a
37	chr19:56363105-56363155	U87	brain:	n/a
38	chr19:56443824-56443874	NT2-D1	testis:	n/a
39	chr19:56348216-56348266	NHDF-neo	bronchial:	n/a
40	chr19:56346743-56346793	ECC-1	luminal epithelium:	n/a
41	chr19:56347771-56347821	HL-60	blood:	n/a
42	chr19:56444163-56444213	HL-60	blood:	n/a
43	chr19:56348889-56348939	BJ	skin:	n/a
44	chr19:56443824-56443874	AoSMC	blood vessel:	n/a
45	chr19:56367316-56367366	HRPEpiC	eye:	n/a
46	chr19:56348216-56348266	ProgFib	skin:	n/a
47	chr19:56346628-56346678	IMR90	lung:	fetal
48	chr19:56393163-56393213	HCT-116	colon:	n/a
49	chr19:56347771-56347821	NT2-D1	testis:	n/a
50	chr19:56348889-56348939	HCM	heart:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:56437345..56439386-chr19:56452694..56454259,2	K562	blood:
2	chr19:56015535..56016051-chr19:56320998..56321733,2	K562	blood:
3	chr19:56327095..56328748-chr19:56329446..56331884,2	K562	blood:
4	chr19:56311206..56314019-chr19:56318458..56321376,2	K562	blood:
5	chr19:56143497..56144412-chr19:56320540..56321434,5	K562	blood:
6	chr19:56164701..56165323-chr19:56320540..56321426,2	MCF-7	breast:
7	chr19:56373661..56375169-chr19:56376696..56378685,2	K562	blood:
8	chr19:56424869..56425718-chr19:56582163..56583125,2	MCF-7	breast:
9	chr19:56154646..56157469-chr19:56320244..56322064,2	K562	blood:
10	chr19:56321292..56324216-chr19:56328648..56330959,2	K562	blood:
11	chr19:56230205..56232527-chr19:56319829..56322446,2	K562	blood:
12	chr19:56320256..56321150-chr19:56577550..56578288,2	K562	blood:
13	chr19:56439351..56441429-chr19:56446067..56448328,2	MCF-7	breast:
14	chr19:56439351..56441429-chr19:56446067..56448328,2	MCF-7	breast:
15	chr19:56288962..56289563-chr19:56320651..56321410,3	MCF-7	breast:
16	chr19:56430402..56432379-chr19:56447676..56449907,2	K562	blood:
17	chr19:56430402..56432379-chr19:56447676..56449907,2	K562	blood:
18	chr19:56373661..56375169-chr19:56376696..56378685,2	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
ENSG00000267522	chromatin interactions
ENSG00000179873	chromatin interactions
ENSG00000171425	chromatin interactions

Extended variants
information (count: 1850 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1850 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7255234	chr19:56319416-56319417	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115331623	chr19:56319447-56319448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558693736	chr19:56319458-56319459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112735283	chr19:56319464-56319465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565240218	chr19:56319468-56319469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532465618	chr19:56319469-56319470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs45565433	chr19:56319502-56319503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111317912	chr19:56319504-56319505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199476238	chr19:56319508-56319509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs299165	chr19:56319525-56319526	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs189778996	chr19:56319528-56319529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199476237	chr19:56319529-56319530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529885719	chr19:56319545-56319546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548018588	chr19:56319546-56319547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10500321	chr19:56319571-56319572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs149258264	chr19:56319572-56319573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533603115	chr19:56319587-56319588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551763858	chr19:56319596-56319597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570079506	chr19:56319607-56319608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538968395	chr19:56319612-56319613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562647596	chr19:56319613-56319614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146366437	chr19:56319697-56319698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531871689	chr19:56319708-56319709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78375736	chr19:56319732-56319733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76514354	chr19:56319757-56319758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529819887	chr19:56319761-56319762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs299164	chr19:56319796-56319797	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs566731999	chr19:56319806-56319807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538640856	chr19:56319831-56319832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558630501	chr19:56319832-56319833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201440877	chr19:56319840-56319841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs199476236	chr19:56319879-56319880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139659204	chr19:56319922-56319923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554347039	chr19:56319940-56319941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181371237	chr19:56319944-56319945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540396643	chr19:56319949-56319950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374532114	chr19:56319963-56319964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75918315	chr19:56319981-56319982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546077846	chr19:56319985-56319986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562574772	chr19:56320045-56320046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540335558	chr19:56320054-56320055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547589714	chr19:56320056-56320057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568017074	chr19:56320061-56320062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199476235	chr19:56320062-56320063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75297296	chr19:56320071-56320072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375951841	chr19:56320089-56320090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542328667	chr19:56320112-56320113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377391099	chr19:56320119-56320120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562006069	chr19:56320126-56320127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138043495	chr19:56320150-56320151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56316200-56320800	Weak transcription	Brain Substantia Nigra	brain
2	chr19:56318800-56319800	Weak transcription	Liver	Liver
3	chr19:56319800-56320600	Enhancers	Liver	Liver
4	chr19:56320200-56321000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
5	chr19:56320400-56320600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr19:56320400-56321000	ZNF genes & repeats	A549	lung
7	chr19:56320400-56321200	Enhancers	GM12878-XiMat	blood
8	chr19:56320600-56320800	Active TSS	Adipose Nuclei	Adipose
9	chr19:56320600-56320800	Flanking Active TSS	Hela-S3	cervix
10	chr19:56320600-56321000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr19:56320600-56321000	Flanking Active TSS	Liver	Liver
12	chr19:56320600-56321000	Active TSS	Duodenum Mucosa	Duodenum
13	chr19:56320600-56321000	Enhancers	Pancreas	Pancrea
14	chr19:56320600-56321000	Active TSS	Rectal Mucosa Donor 29	rectum
15	chr19:56320600-56321000	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr19:56320600-56321000	Flanking Active TSS	K562	blood
17	chr19:56320600-56321400	Enhancers	Primary B cells from peripheral blood	blood
18	chr19:56320800-56321000	Flanking Active TSS	Adipose Nuclei	Adipose
19	chr19:56320800-56321000	ZNF genes & repeats	Fetal Intestine Small	intestine
20	chr19:56320800-56321000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
21	chr19:56320800-56321200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr19:56320800-56321200	Bivalent Enhancer	Brain Anterior Caudate	brain
23	chr19:56320800-56321200	Active TSS	Hela-S3	cervix
24	chr19:56320800-56321400	Active TSS	Brain Substantia Nigra	brain
25	chr19:56321000-56321400	Enhancers	Liver	Liver
26	chr19:56321000-56321400	Enhancers	K562	blood
27	chr19:56321000-56323000	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr19:56321200-56321400	Flanking Active TSS	Hela-S3	cervix
29	chr19:56329400-56330200	Enhancers	GM12878-XiMat	blood
30	chr19:56329600-56334200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
31	chr19:56330200-56331800	Flanking Active TSS	GM12878-XiMat	blood
32	chr19:56330200-56332000	Enhancers	Primary B cells from peripheral blood	blood
33	chr19:56331200-56331800	Active TSS	Rectal Mucosa Donor 29	rectum
34	chr19:56331800-56332600	Enhancers	GM12878-XiMat	blood
35	chr19:56333400-56334000	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr19:56333800-56334200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr19:56333800-56334200	Active TSS	Primary T cells fromperipheralblood	blood
38	chr19:56342200-56342600	Active TSS	HSMM	muscle
39	chr19:56347600-56348200	Active TSS	A549	lung
40	chr19:56357800-56358000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr19:56359400-56361200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr19:56360400-56361000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr19:56360400-56361400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
44	chr19:56363400-56364600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
45	chr19:56364600-56372200	Enhancers	Primary B cells from peripheral blood	blood
46	chr19:56365200-56365400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr19:56366400-56366800	Enhancers	GM12878-XiMat	blood
48	chr19:56366800-56367000	Flanking Active TSS	GM12878-XiMat	blood
49	chr19:56367000-56367200	Enhancers	GM12878-XiMat	blood
50	chr19:56367200-56367400	Flanking Active TSS	GM12878-XiMat	blood

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