Variant report

Variant	esv18275
Chromosome Location	chr20:29528858-29580700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr20:29557150-29557425	GM12878	blood:	n/a	n/a
2	BCL11A	chr20:29543803-29543974	GM12878	blood:	n/a	n/a
3	BHLHE40	chr20:29570929-29571032	K562	blood:	n/a	n/a
4	CTCF	chr20:29535660-29535810	RPTEC	kidney:	n/a	n/a
5	CTCF	chr20:29535629-29535737	K562	blood:	n/a	n/a
6	CTCF	chr20:29538580-29538730	WI-38	lung:	n/a	n/a
7	CTCF	chr20:29535620-29535770	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr20:29535660-29535810	HCM	heart:	n/a	n/a
9	CTCF	chr20:29535660-29535810	Caco-2	colon:	n/a	n/a
10	CTCF	chr20:29560485-29560520	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr20:29547617-29547703	GM10248	blood:	n/a	n/a
12	CTCF	chr20:29535620-29535770	HepG2	liver:	n/a	n/a
13	CTCF	chr20:29531202-29531231	GM20000	blood:	n/a	n/a
14	CTCF	chr20:29535640-29535790	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr20:29544606-29544676	GM10248	blood:	n/a	n/a
16	CTCF	chr20:29535626-29535771	K562	blood:	n/a	n/a
17	E2F6	chr20:29570890-29571093	K562	blood:	n/a	n/a
18	EBF1	chr20:29557233-29557426	GM12878	blood:	n/a	n/a
19	EBF1	chr20:29556671-29556868	GM12878	blood:	n/a	n/a
20	ELF1	chr20:29572765-29572951	K562	blood:	n/a	n/a
21	EP300	chr20:29539975-29540338	GM12878	blood:	n/a	n/a
22	EP300	chr20:29536240-29536529	GM12878	blood:	n/a	n/a
23	EP300	chr20:29575587-29575756	GM12878	blood:	n/a	n/a
24	EP300	chr20:29577970-29578223	GM12878	blood:	n/a	n/a
25	EP300	chr20:29538686-29538970	GM12878	blood:	n/a	n/a
26	EP300	chr20:29534163-29534503	GM12878	blood:	n/a	n/a
27	EP300	chr20:29541656-29541915	GM12878	blood:	n/a	n/a
28	FOSL2	chr20:29532571-29532891	HepG2	liver:	n/a	n/a
29	FOSL2	chr20:29537381-29537636	HepG2	liver:	n/a	n/a
30	FOSL2	chr20:29536307-29536578	HepG2	liver:	n/a	n/a
31	FOSL2	chr20:29571451-29572093	HepG2	liver:	n/a	n/a
32	FOXA1	chr20:29532506-29532995	HepG2	liver:	n/a	n/a
33	GABPA	chr20:29536226-29536589	Hela-S3	cervix:	n/a	n/a
34	GABPA	chr20:29554590-29554810	Hela-S3	cervix:	n/a	n/a
35	GABPA	chr20:29541675-29541798	Hela-S3	cervix:	n/a	n/a
36	GABPA	chr20:29569266-29569492	Hela-S3	cervix:	n/a	n/a
37	GATA2	chr20:29531874-29532131	K562	blood:	n/a	chr20:29531990-29531999 chr20:29531990-29532000 chr20:29531987-29532003 chr20:29531992-29531999
38	IRF4	chr20:29562839-29563284	GM12878	blood:	n/a	n/a
39	JUND	chr20:29543857-29543994	HepG2	liver:	n/a	n/a
40	JUND	chr20:29540053-29540230	HepG2	liver:	n/a	n/a
41	JUND	chr20:29532678-29532802	HepG2	liver:	n/a	n/a
42	JUND	chr20:29563078-29563199	HepG2	liver:	n/a	n/a
43	MAFF	chr20:29547033-29547232	HepG2	liver:	n/a	n/a
44	MAFK	chr20:29547046-29547212	IMR90	lung:	n/a	chr20:29547113-29547124 chr20:29547112-29547123 chr20:29547108-29547123 chr20:29547113-29547124 chr20:29547112-29547123 chr20:29547108-29547124
45	MAFK	chr20:29547048-29547222	HepG2	liver:	n/a	chr20:29547113-29547124 chr20:29547112-29547123 chr20:29547108-29547123 chr20:29547113-29547124 chr20:29547112-29547123 chr20:29547108-29547124
46	MAFK	chr20:29547029-29547238	HepG2	liver:	n/a	chr20:29547113-29547124 chr20:29547112-29547123 chr20:29547108-29547123 chr20:29547113-29547124 chr20:29547112-29547123 chr20:29547108-29547124
47	MAX	chr20:29570368-29570596	K562	blood:	n/a	chr20:29570485-29570494 chr20:29570484-29570495 chr20:29570484-29570495 chr20:29570485-29570494 chr20:29570484-29570495 chr20:29570481-29570496 chr20:29570483-29570496 chr20:29570483-29570496 chr20:29570484-29570494 chr20:29570483-29570496 chr20:29570480-29570499 chr20:29570485-29570495 chr20:29570485-29570494 chr20:29570485-29570495 chr20:29570486-29570495 chr20:29570484-29570494
48	MAX	chr20:29570857-29571083	K562	blood:	n/a	n/a
49	MAX	chr20:29570771-29571171	K562	blood:	n/a	n/a
50	MAX	chr20:29570876-29571040	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:29535056-29535106	AG04449	skin:	fetal
2	chr20:29551422-29551472	HCM	heart:	n/a
3	chr20:29535013-29535063	HMEC	breast:	n/a
4	chr20:29535056-29535106	AG04449	skin:	fetal
5	chr20:29551422-29551472	HCM	heart:	n/a
6	chr20:29535013-29535063	HMEC	breast:	n/a
7	chr20:29549396-29549446	U87	brain:	n/a
8	chr20:29534074-29534124	AG04449	skin:	fetal
9	chr20:29535150-29535200	HCT-116	colon:	n/a
10	chr20:29550850-29550900	HRPEpiC	eye:	n/a
11	chr20:29537189-29537239	A549	lung:	n/a
12	chr20:29537189-29537239	NT2-D1	testis:	n/a
13	chr20:29535150-29535200	HRPEpiC	eye:	n/a
14	chr20:29534074-29534124	SAEC	small airway:	n/a
15	chr20:29549396-29549446	Hepatocyte	liver:	n/a
16	chr20:29538155-29538205	AG10803	skin:	n/a
17	chr20:29535056-29535106	HAEpiC	amniotic membrane:	n/a
18	chr20:29547097-29547147	PANC-1	pancreas:	n/a
19	chr20:29547097-29547147	H1-hESC	embryonic stem cell:	embryo
20	chr20:29535150-29535200	NB4	blood:	n/a
21	chr20:29549396-29549446	HMEC	breast:	n/a
22	chr20:29535013-29535063	PANC-1	pancreas:	n/a
23	chr20:29535007-29535057	GM12878	blood:	n/a
24	chr20:29547097-29547147	HUVEC	blood vessel:	n/a
25	chr20:29554089-29554139	HepG2	liver:	n/a
26	chr20:29535007-29535057	GM12892	blood:	n/a
27	chr20:29554089-29554139	SK-N-SH_RA	brain:	n/a
28	chr20:29535013-29535063	Hela-S3	cervix:	n/a
29	chr20:29537189-29537239	BE2_C	brain:	n/a
30	chr20:29535007-29535057	AG10803	skin:	n/a
31	chr20:29554089-29554139	SKMC	muscle:	n/a
32	chr20:29547097-29547147	Hela-S3	cervix:	n/a
33	chr20:29551422-29551472	GM19239	blood:	n/a
34	chr20:29551422-29551472	SK-N-SH_RA	brain:	n/a
35	chr20:29551622-29551672	HCF	heart:	n/a
36	chr20:29551422-29551472	NT2-D1	testis:	n/a
37	chr20:29534074-29534124	HMEC	breast:	n/a
38	chr20:29554089-29554139	T-47D	breast:	n/a
39	chr20:29551422-29551472	SKMC	muscle:	n/a
40	chr20:29534074-29534124	SK-N-MC	brain:	n/a
41	chr20:29537189-29537239	HEK293	kidney:	embryo
42	chr20:29554089-29554139	RPTEC	kidney:	n/a
43	chr20:29535150-29535200	HPAEpiC	pulmonary alveolar:	n/a
44	chr20:29538155-29538205	SK-N-MC	brain:	n/a
45	chr20:29537189-29537239	GM06990	blood:	n/a
46	chr20:29551622-29551672	A549	lung:	n/a
47	chr20:29554089-29554139	PrEC	prostate:	n/a
48	chr20:29547097-29547147	PFSK-1	brain:	n/a
49	chr20:29537189-29537239	HNPCEpiC	eye:	n/a
50	chr20:29535150-29535200	Caco-2	colon:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB116-1	chr20:29565784-29565927	ENSG00000231934.1
2	lnc-DEFB116-1	chr20:29559468-29559502	XLOC_013717
3	lnc-DEFB116-1	chr20:29570232-29570484	NONHSAT079273
4	lnc-DEFB116-1	chr20:29565782-29565935	NONHSAT079273
5	lnc-DEFB116-1	chr20:29565756-29565927	ENSG00000231934.1
6	lnc-DEFB116-1	chr20:29559203-29559502	ENSG00000231934.1
7	lnc-DEFB116-1	chr20:29570224-29570363	ENSG00000231934.1
8	lnc-DEFB116-1	chr20:29558488-29558622	ENSG00000231934.1
9	lnc-DEFB116-1	chr20:29565784-29565969	XLOC_013717

Variant related genes	Relation type
ENSG00000200325	TF binding region
ENSG00000231934	TF binding region
ENSG00000200325	CpG island
ENSG00000231934	CpG island
RIMS3	miRNA target sites
RICTOR	miRNA target sites

Extended variants
information (count: 2337 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2337 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543383762	chr20:29528877-29528878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371366306	chr20:29528901-29528902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188624286	chr20:29528916-29528917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200276889	chr20:29528935-29528936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374622548	chr20:29528943-29528944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181647609	chr20:29528952-29528953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10427434	chr20:29528953-29528954	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs543362398	chr20:29528960-29528961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555299895	chr20:29528976-29528977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368220044	chr20:29528985-29528986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371984778	chr20:29528995-29528996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563453613	chr20:29529004-29529005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529089683	chr20:29529029-29529030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549030590	chr20:29529030-29529031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576739358	chr20:29529032-29529033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543979987	chr20:29529057-29529058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6087205	chr20:29529068-29529069	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs528215727	chr20:29529156-29529157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141587171	chr20:29529181-29529182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79047428	chr20:29529229-29529230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571301622	chr20:29529256-29529257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540133928	chr20:29529275-29529276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550498637	chr20:29529289-29529290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75676357	chr20:29529291-29529292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570191000	chr20:29529307-29529308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535692669	chr20:29529327-29529328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139702854	chr20:29529350-29529351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs57835703	chr20:29529357-29529358	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs186780915	chr20:29529365-29529366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557729108	chr20:29529369-29529370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374460195	chr20:29529370-29529371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577620299	chr20:29529375-29529376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543275162	chr20:29529405-29529406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371741532	chr20:29529434-29529435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563452311	chr20:29529441-29529442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573749708	chr20:29529444-29529445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192089609	chr20:29529492-29529493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs544729666	chr20:29529501-29529502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528182904	chr20:29529507-29529508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183850159	chr20:29529519-29529520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564822829	chr20:29529536-29529537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146605324	chr20:29529541-29529542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139114268	chr20:29529565-29529566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149899538	chr20:29529570-29529571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375837390	chr20:29529585-29529586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570232521	chr20:29529587-29529588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186563160	chr20:29529617-29529618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144905707	chr20:29529627-29529628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149024746	chr20:29529642-29529643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1811869	chr20:29529644-29529645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21806811	CNVD
Melanoma	21693616	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Soft tissue tumor	16732325	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	22860045	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Amyotrophic lateral sclerosis	20688871	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:29521000-29534000	Weak transcription	Gastric	stomach
2	chr20:29524800-29535000	Weak transcription	Pancreas	Pancrea
3	chr20:29525000-29535200	Weak transcription	Small Intestine	intestine
4	chr20:29525600-29529600	Weak transcription	Duodenum Mucosa	Duodenum
5	chr20:29525600-29531000	Weak transcription	Stomach Mucosa	stomach
6	chr20:29525600-29535200	Weak transcription	Right Atrium	heart
7	chr20:29527600-29529600	Enhancers	K562	blood
8	chr20:29529600-29530000	Enhancers	Duodenum Mucosa	Duodenum
9	chr20:29530000-29533400	Weak transcription	Duodenum Mucosa	Duodenum
10	chr20:29531000-29532200	Enhancers	Stomach Mucosa	stomach
11	chr20:29533400-29534800	Enhancers	Duodenum Mucosa	Duodenum
12	chr20:29534000-29534200	Enhancers	Gastric	stomach
13	chr20:29534600-29535000	Active TSS	Stomach Smooth Muscle	stomach
14	chr20:29534600-29535200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
15	chr20:29534600-29535200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr20:29534800-29535000	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr20:29534800-29535000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr20:29534800-29535000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr20:29534800-29535000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
20	chr20:29534800-29535000	Flanking Active TSS	Duodenum Mucosa	Duodenum
21	chr20:29534800-29535200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
22	chr20:29534800-29535200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr20:29534800-29535200	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr20:29534800-29535200	Active TSS	Colonic Mucosa	Colon
25	chr20:29534800-29535200	Active TSS	Duodenum Smooth Muscle	Duodenum
26	chr20:29534800-29535200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
27	chr20:29534800-29535400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr20:29534800-29535400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
29	chr20:29534800-29535400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
30	chr20:29534800-29535400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
31	chr20:29534800-29535400	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr20:29534800-29535400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
33	chr20:29534800-29535400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr20:29535000-29535200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr20:29535000-29535200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr20:29535000-29535200	Enhancers	Pancreas	Pancrea
37	chr20:29535000-29535400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
38	chr20:29535000-29535400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
39	chr20:29535000-29535400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr20:29535200-29535400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr20:29535200-29535400	Enhancers	Small Intestine	intestine
42	chr20:29535400-29535800	Enhancers	Primary T cells fromperipheralblood	blood
43	chr20:29535400-29535800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr20:29536800-29537600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
45	chr20:29537200-29537600	Enhancers	K562	blood
46	chr20:29537600-29537800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr20:29543600-29546000	Enhancers	Duodenum Mucosa	Duodenum
48	chr20:29546000-29548000	Weak transcription	Duodenum Mucosa	Duodenum
49	chr20:29548000-29549000	Enhancers	Duodenum Mucosa	Duodenum
50	chr20:29549000-29549200	Flanking Bivalent TSS/Enh	Sigmoid Colon	Sigmoid Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links