Variant report

Variant	nsv1060197
Chromosome Location	chr22:29817507-29842511
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:95)
CpG islands
(count:854)
Chromatin interactive
region (count:3)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:95 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr22:29838923-29839071	GM12878	blood:	n/a	chr22:29838978-29838989
2	CEBPB	chr22:29828110-29828269	K562	blood:	n/a	n/a
3	CEBPB	chr22:29839063-29839837	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr22:29837127-29837219	HepG2	liver:	n/a	chr22:29837132-29837143
5	CEBPB	chr22:29828051-29828325	K562	blood:	n/a	n/a
6	CEBPB	chr22:29837053-29837238	K562	blood:	n/a	chr22:29837132-29837143
7	CTCF	chr22:29817578-29817695	GM12892	blood:	n/a	n/a
8	CTCF	chr22:29828159-29828241	Lung_OC	lung:	n/a	n/a
9	CTCF	chr22:29823099-29823128	HepG2	liver:	n/a	n/a
10	CTCF	chr22:29817436-29817744	K562	blood:	n/a	n/a
11	CTCF	chr22:29817566-29817669	MCF-7	breast:	n/a	n/a
12	CTCF	chr22:29817521-29817688	K562	blood:	n/a	n/a
13	CTCF	chr22:29817595-29817708	GM19239	blood:	n/a	n/a
14	CTCF	chr22:29817536-29817634	GM10248	blood:	n/a	n/a
15	CTCF	chr22:29819237-29819257	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr22:29817564-29817682	Gliobla	brain:	n/a	n/a
17	CTCF	chr22:29817562-29817711	GM19238	blood:	n/a	n/a
18	CTCF	chr22:29817618-29817639	A549	lung:	n/a	n/a
19	CTCF	chr22:29817556-29817711	HepG2	liver:	n/a	n/a
20	CTCF	chr22:29817400-29817550	GM12872	blood:	n/a	n/a
21	CTCF	chr22:29817515-29817727	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr22:29837885-29837943	GM13976	blood:	n/a	n/a
23	CTCF	chr22:29817598-29817685	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr22:29819250-29819253	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr22:29832287-29832310	Lung_OC	lung:	n/a	n/a
26	CTCF	chr22:29817580-29817719	GM12891	blood:	n/a	n/a
27	CTCF	chr22:29823078-29823172	MCF-7	breast:	n/a	chr22:29823094-29823112
28	CTCF	chr22:29823000-29823150	K562	blood:	n/a	chr22:29823094-29823112
29	CTCF	chr22:29825861-29825916	HepG2	liver:	n/a	n/a
30	CTCF	chr22:29817519-29817703	K562	blood:	n/a	n/a
31	CTCF	chr22:29823057-29823128	MCF-7	breast:	n/a	chr22:29823094-29823112
32	CTCF	chr22:29823064-29823140	Hela-S3	cervix:	n/a	chr22:29823094-29823112
33	CTCF	chr22:29834556-29834610	Lung_OC	lung:	n/a	n/a
34	CTCF	chr22:29817683-29817685	Gliobla	brain:	n/a	n/a
35	CTCF	chr22:29817592-29817678	NHEK	skin:	n/a	n/a
36	CTCF	chr22:29817595-29817681	MCF-7	breast:	n/a	n/a
37	CTCF	chr22:29825832-29825926	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr22:29833658-29833700	MCF-7	breast:	n/a	n/a
39	CTCF	chr22:29825837-29825925	K562	blood:	n/a	n/a
40	CTCF	chr22:29817548-29817669	GM19240	blood:	n/a	n/a
41	CTCF	chr22:29819259-29819285	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr22:29825740-29825890	BE2_C	brain:	n/a	n/a
43	CTCF	chr22:29823103-29823162	MCF-7	breast:	n/a	n/a
44	CTCF	chr22:29817576-29817690	GM12878	blood:	n/a	n/a
45	CTCF	chr22:29825220-29825370	BE2_C	brain:	n/a	n/a
46	CTCF	chr22:29840080-29840230	GM12867	blood:	n/a	n/a
47	CTCF	chr22:29823008-29823185	K562	blood:	n/a	chr22:29823094-29823112
48	CTCF	chr22:29819215-29819241	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr22:29823000-29823150	MCF-7	breast:	n/a	chr22:29823094-29823112
50	EP300	chr22:29839556-29840000	Hela-S3	cervix:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29837794-29837844	Hepatocyte	liver:	n/a
2	chr22:29833658-29833708	GM12891	blood:	n/a
3	chr22:29838869-29838919	AG04449	skin:	fetal
4	chr22:29834388-29834438	U87	brain:	n/a
5	chr22:29834420-29834470	HRCEpiC	kidney:	n/a
6	chr22:29833804-29833854	GM12878	blood:	n/a
7	chr22:29838193-29838243	PrEC	prostate:	n/a
8	chr22:29834697-29834747	RPTEC	kidney:	n/a
9	chr22:29833804-29833854	HRCEpiC	kidney:	n/a
10	chr22:29838184-29838234	K562	blood:	n/a
11	chr22:29833804-29833854	NT2-D1	testis:	n/a
12	chr22:29833804-29833854	ProgFib	skin:	n/a
13	chr22:29838687-29838737	ProgFib	skin:	n/a
14	chr22:29838869-29838919	HEK293	kidney:	embryo
15	chr22:29834657-29834707	PFSK-1	brain:	n/a
16	chr22:29834388-29834438	HRPEpiC	eye:	n/a
17	chr22:29834657-29834707	ProgFib	skin:	n/a
18	chr22:29834550-29834600	ovcar-3	ovarian:	n/a
19	chr22:29838869-29838919	HCM	heart:	n/a
20	chr22:29839545-29839595	AG04450	lung:	fetal
21	chr22:29833658-29833708	U87	brain:	n/a
22	chr22:29839545-29839595	HCPEpiC	choroid plexus:	n/a
23	chr22:29834550-29834600	T-47D	breast:	n/a
24	chr22:29838193-29838243	NHBE	bronchial:	n/a
25	chr22:29838193-29838243	HRE	kidney:	n/a
26	chr22:29833658-29833708	NB4	blood:	n/a
27	chr22:29838687-29838737	NB4	blood:	n/a
28	chr22:29834697-29834747	SK-N-MC	brain:	n/a
29	chr22:29834657-29834707	GM12892	blood:	n/a
30	chr22:29834697-29834747	AG04450	lung:	fetal
31	chr22:29838655-29838705	SKMC	muscle:	n/a
32	chr22:29837794-29837844	T-47D	breast:	n/a
33	chr22:29837794-29837844	HIPEpiC	eye:	n/a
34	chr22:29833804-29833854	SK-N-MC	brain:	n/a
35	chr22:29838869-29838919	HCT-116	colon:	n/a
36	chr22:29838184-29838234	NHBE	bronchial:	n/a
37	chr22:29834657-29834707	SK-N-SH_RA	brain:	n/a
38	chr22:29834697-29834747	SKMC	muscle:	n/a
39	chr22:29834550-29834600	AG09319	gingival:	n/a
40	chr22:29834388-29834438	BE2_C	brain:	n/a
41	chr22:29838655-29838705	AoSMC	blood vessel:	n/a
42	chr22:29834388-29834438	GM12891	blood:	n/a
43	chr22:29839545-29839595	SAEC	small airway:	n/a
44	chr22:29838687-29838737	Caco-2	colon:	n/a
45	chr22:29834388-29834438	K562	blood:	n/a
46	chr22:29834420-29834470	PrEC	prostate:	n/a
47	chr22:29834697-29834747	AG09319	gingival:	n/a
48	chr22:29838869-29838919	SAEC	small airway:	n/a
49	chr22:29834388-29834438	HRCEpiC	kidney:	n/a
50	chr22:29838655-29838705	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr22:29777011..29779930-chr22:29821335..29822984,2	K562	blood:
2	chr22:29842498..29846304-chr22:29847549..29850894,5	K562	blood:
3	chr22:29838351..29841311-chr22:29875165..29877820,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP1B1-1	chr22:29832818-29838118	ENSG00000225465.6
2	lnc-AP1B1-1	chr22:29837564-29838118	NONHSAT084706
3	lnc-AP1B1-1	chr22:29837244-29837827	ENSG00000225465.4
4	lnc-AP1B1-1	chr22:29833016-29838118	NONHSAT084704
5	lnc-AP1B1-1	chr22:29832818-29838118	NONHSAT084700
6	lnc-AP1B1-1	chr22:29833004-29838118	NONHSAT084701
7	lnc-AP1B1-1	chr22:29833006-29838118	ENSG00000225465.4
8	lnc-AP1B1-1	chr22:29833007-29838118	NONHSAT084702
9	lnc-AP1B1-1	chr22:29833007-29838118	NONHSAT084703

No data

Variant related genes	Relation type
RFPL1	TF binding region
ENSG00000242156	TF binding region
RFPL1S	TF binding region
AP1B1	TF binding region
RFPL1	CpG island
ENSG00000242156	CpG island
RFPL1S	CpG island
AP1B1	CpG island
ENSG00000100285	chromatin interactions

Extended variants
information (count: 1018 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1018 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117617130	chr22:29817516-29817517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs540568601	chr22:29817549-29817550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371604284	chr22:29817588-29817589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150370048	chr22:29817644-29817645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535493563	chr22:29817666-29817667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557278435	chr22:29817668-29817669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145126493	chr22:29817689-29817690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371338151	chr22:29817746-29817747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532806093	chr22:29817763-29817764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377254605	chr22:29817765-29817766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558008619	chr22:29817767-29817768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573094385	chr22:29817786-29817787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs367928220	chr22:29817856-29817857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113024742	chr22:29817859-29817860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573934657	chr22:29817911-29817912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543916734	chr22:29817912-29817913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375749542	chr22:29817941-29817942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532920710	chr22:29818000-29818001	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs371809581	chr22:29818001-29818002	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs376364611	chr22:29818006-29818007	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs620388	chr22:29818044-29818045	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs182639726	chr22:29818045-29818046	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs528678759	chr22:29818094-29818095	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs545075703	chr22:29818096-29818097	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs568419896	chr22:29818097-29818098	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs369599705	chr22:29818100-29818101	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs550732016	chr22:29818105-29818106	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs143046688	chr22:29818220-29818221	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs112549094	chr22:29818291-29818292	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs146131266	chr22:29818393-29818394	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs566929981	chr22:29818395-29818396	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs533977836	chr22:29818456-29818457	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs373789846	chr22:29818470-29818471	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs187201340	chr22:29818480-29818481	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs573894340	chr22:29818491-29818492	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs544480695	chr22:29818495-29818496	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs200970895	chr22:29818504-29818505	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs373540429	chr22:29818536-29818537	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs555914912	chr22:29818575-29818576	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs577588462	chr22:29818579-29818580	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs191319218	chr22:29818601-29818602	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs544647699	chr22:29818605-29818606	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs559827187	chr22:29818618-29818619	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs184415565	chr22:29818629-29818630	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs6006138	chr22:29818689-29818690	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530949407	chr22:29818698-29818699	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs6006139	chr22:29818708-29818709	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs561929539	chr22:29818710-29818711	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs529585955	chr22:29818724-29818725	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs551276326	chr22:29818733-29818734	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29811600-29823200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr22:29815400-29818600	Enhancers	Primary B cells from peripheral blood	blood
3	chr22:29815800-29818200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr22:29816000-29818000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr22:29816200-29818600	Enhancers	Primary B cells from cord blood	blood
6	chr22:29816400-29818200	Weak transcription	K562	blood
7	chr22:29816400-29818400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr22:29816800-29818000	Weak transcription	Spleen	Spleen
9	chr22:29817200-29818000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr22:29818000-29818200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr22:29818000-29818400	Enhancers	Spleen	Spleen
12	chr22:29818000-29818800	Enhancers	Primary hematopoietic stem cells	blood
13	chr22:29818200-29818600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr22:29818200-29818600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr22:29818400-29818600	Enhancers	K562	blood
16	chr22:29818400-29818800	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr22:29818600-29819000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr22:29818600-29819000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr22:29823000-29824000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr22:29823200-29823400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr22:29823200-29824000	Enhancers	NHDF-Ad	bronchial
22	chr22:29823400-29823600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr22:29826600-29827600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr22:29826800-29827400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr22:29826800-29827400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr22:29826800-29828400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr22:29827000-29827400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr22:29827000-29827600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr22:29827200-29827400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr22:29827200-29827600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr22:29827200-29828400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr22:29827200-29828400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr22:29827200-29828800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr22:29827200-29828800	Enhancers	Fetal Intestine Small	intestine
35	chr22:29827200-29829000	Enhancers	Fetal Intestine Large	intestine
36	chr22:29827400-29828200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr22:29827600-29827800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr22:29827600-29828000	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr22:29827600-29828600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr22:29827600-29828600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr22:29827800-29828000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr22:29828000-29828200	Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr22:29828000-29828600	Enhancers	K562	blood
44	chr22:29828000-29829000	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr22:29828200-29828400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr22:29828200-29828600	Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr22:29828400-29829000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr22:29828600-29828800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr22:29828600-29828800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr22:29828600-29829000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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