Variant report

Variant	esv11702
Chromosome Location	chr21:40981640-40987483
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:115)
CpG islands
(count:611)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:115 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr21:40982540-40983012	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr21:40982496-40982970	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr21:40985244-40985498	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr21:40984949-40984971	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr21:40985549-40985749	K562	blood:	n/a	n/a
6	CHD1	chr21:40983959-40984159	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr21:40985461-40985984	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD1	chr21:40984373-40984511	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr21:40983481-40983811	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr21:40984082-40984890	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr21:40984780-40984930	Caco-2	colon:	n/a	n/a
12	CTCF	chr21:40984780-40984930	AG09319	gingival:	n/a	n/a
13	CTCF	chr21:40984800-40984950	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr21:40984840-40984990	HEK293	kidney:	n/a	n/a
15	CTCF	chr21:40984299-40984374	Fibrobl	skin:	n/a	n/a
16	CTCF	chr21:40984840-40984990	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr21:40984802-40984968	MCF-7	breast:	n/a	n/a
18	CTCF	chr21:40986740-40986890	HRE	kidney:	n/a	n/a
19	CTCF	chr21:40984780-40984930	AG04449	skin:	n/a	n/a
20	CTCF	chr21:40984820-40984970	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr21:40984800-40984950	RPTEC	kidney:	n/a	n/a
22	CTCF	chr21:40984700-40984850	HA-sp	spinal cord:	n/a	n/a
23	CTCF	chr21:40984836-40984932	MCF-7	breast:	n/a	n/a
24	CTCF	chr21:40984838-40984940	MCF-7	breast:	n/a	n/a
25	CTCF	chr21:40984860-40985010	AG04449	skin:	n/a	n/a
26	CTCF	chr21:40984220-40984370	AG09309	skin:	n/a	n/a
27	CTCF	chr21:40984878-40984916	MCF-7	breast:	n/a	n/a
28	CTCF	chr21:40984800-40984950	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr21:40984820-40984970	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr21:40984780-40984930	SK-N-SH_RA	brain:	n/a	n/a
31	E2F6	chr21:40983369-40984008	H1-hESC	embryonic stem cell:	n/a	n/a
32	FOXA1	chr21:40982595-40982859	T-47D	breast:	n/a	n/a
33	FOXA1	chr21:40982649-40982858	ECC-1	luminal epithelium:	n/a	n/a
34	GATA3	chr21:40985802-40986091	MCF-7	breast:	n/a	n/a
35	GATA3	chr21:40985350-40986224	MCF-7	breast:	n/a	n/a
36	GTF2F1	chr21:40984759-40984940	H1-hESC	embryonic stem cell:	n/a	n/a
37	GTF2F1	chr21:40984357-40984543	H1-hESC	embryonic stem cell:	n/a	n/a
38	HA-E2F1	chr21:40985191-40985843	MCF-7	breast:	n/a	n/a
39	IRF1	chr21:40982608-40982758	K562	blood:	n/a	n/a
40	JUN	chr21:40982614-40983146	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUND	chr21:40983623-40983733	H1-hESC	embryonic stem cell:	n/a	n/a
42	JUND	chr21:40984850-40984987	H1-hESC	embryonic stem cell:	n/a	n/a
43	JUND	chr21:40982572-40982960	H1-hESC	embryonic stem cell:	n/a	n/a
44	JUND	chr21:40982557-40983221	H1-hESC	embryonic stem cell:	n/a	n/a
45	JUND	chr21:40984189-40984902	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUND	chr21:40982603-40982940	H1-hESC	embryonic stem cell:	n/a	n/a
47	KAP1	chr21:40982550-40982948	U2OS	brain:	n/a	n/a
48	KAP1	chr21:40985260-40985856	HEK293	kidney:	n/a	n/a
49	MAX	chr21:40982609-40982915	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAX	chr21:40984561-40985053	H1-hESC	embryonic stem cell:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:40985387-40985437	U87	brain:	n/a
2	chr21:40985387-40985437	U87	brain:	n/a
3	chr21:40984610-40984660	HCT-116	colon:	n/a
4	chr21:40984700-40984750	NHDF-neo	bronchial:	n/a
5	chr21:40984553-40984603	A549	lung:	n/a
6	chr21:40984780-40984830	SK-N-MC	brain:	n/a
7	chr21:40984886-40984936	AG09309	skin:	n/a
8	chr21:40984700-40984750	HEEpiC	esophagus:	n/a
9	chr21:40984610-40984660	AG04449	skin:	fetal
10	chr21:40984780-40984830	HEEpiC	esophagus:	n/a
11	chr21:40984777-40984827	GM12891	blood:	n/a
12	chr21:40984763-40984813	HEEpiC	esophagus:	n/a
13	chr21:40984760-40984810	SK-N-SH	brain:	n/a
14	chr21:40984553-40984603	Hela-S3	cervix:	n/a
15	chr21:40984886-40984936	PrEC	prostate:	n/a
16	chr21:40984763-40984813	HNPCEpiC	eye:	n/a
17	chr21:40985406-40985456	HCF	heart:	n/a
18	chr21:40985387-40985437	HRPEpiC	eye:	n/a
19	chr21:40985387-40985437	HMEC	breast:	n/a
20	chr21:40984700-40984750	HAEpiC	amniotic membrane:	n/a
21	chr21:40985406-40985456	SK-N-SH_RA	brain:	n/a
22	chr21:40984553-40984603	HCPEpiC	choroid plexus:	n/a
23	chr21:40984760-40984810	RPTEC	kidney:	n/a
24	chr21:40984760-40984810	U87	brain:	n/a
25	chr21:40984777-40984827	Hela-S3	cervix:	n/a
26	chr21:40985406-40985456	HCPEpiC	choroid plexus:	n/a
27	chr21:40984610-40984660	GM12892	blood:	n/a
28	chr21:40984763-40984813	H1-hESC	embryonic stem cell:	embryo
29	chr21:40984780-40984830	HL-60	blood:	n/a
30	chr21:40984780-40984830	SAEC	small airway:	n/a
31	chr21:40985406-40985456	HL-60	blood:	n/a
32	chr21:40984610-40984660	HEEpiC	esophagus:	n/a
33	chr21:40984700-40984750	NHBE	bronchial:	n/a
34	chr21:40984763-40984813	T-47D	breast:	n/a
35	chr21:40984700-40984750	U87	brain:	n/a
36	chr21:40984553-40984603	AG04449	skin:	fetal
37	chr21:40984610-40984660	ovcar-3	ovarian:	n/a
38	chr21:40984780-40984830	Caco-2	colon:	n/a
39	chr21:40984760-40984810	Caco-2	colon:	n/a
40	chr21:40984886-40984936	GM12891	blood:	n/a
41	chr21:40984760-40984810	Jurkat	blood:	n/a
42	chr21:40984780-40984830	HCM	heart:	n/a
43	chr21:40984780-40984830	ECC-1	luminal epithelium:	n/a
44	chr21:40984763-40984813	AG10803	skin:	n/a
45	chr21:40985387-40985437	NB4	blood:	n/a
46	chr21:40984610-40984660	HepG2	liver:	n/a
47	chr21:40985406-40985456	Hela-S3	cervix:	n/a
48	chr21:40984610-40984660	HNPCEpiC	eye:	n/a
49	chr21:40984760-40984810	LNCaP	prostate:	n/a
50	chr21:40984760-40984810	HCPEpiC	choroid plexus:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:40985808..40987789-chr21:41000169..41002424,2	MCF-7	breast:
2	chr21:40980416..40982821-chr21:40984581..40986944,3	MCF-7	breast:
3	chr21:40982969..40984570-chr21:40986006..40988233,2	MCF-7	breast:
4	chr21:40986802..40989122-chr21:41045623..41048115,2	MCF-7	breast:
5	chr21:40979099..40981850-chr21:40982315..40985666,4	MCF-7	breast:
6	chr21:40950925..40952824-chr21:40985213..40987161,2	MCF-7	breast:
7	chr21:40895232..40897422-chr21:40987219..40990019,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C21orf88-1	chr21:40984224-40984994	NONHSAT082200
2	lnc-C21orf88-1	chr21:40984224-40984749	NR_026543
3	lnc-C21orf88-1	chr21:40984224-40984749	NR_026542

No data

Variant related genes	Relation type
C21orf88	TF binding region
C21orf88	CpG island
ENSG00000225330	chromatin interactions
ENSG00000184809	chromatin interactions

Extended variants
information (count: 221 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:221 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542450669	chr21:40981663-40981664	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs562321429	chr21:40981698-40981699	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs181896963	chr21:40981701-40981702	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs543825564	chr21:40981703-40981704	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs564091411	chr21:40981770-40981771	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550569	chr21:40981775-40981776	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs546673815	chr21:40981788-40981789	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566274115	chr21:40981830-40981831	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs529016814	chr21:40981831-40981832	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs548772565	chr21:40981841-40981842	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545396342	chr21:40981894-40981895	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs372975965	chr21:40981898-40981899	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs557803387	chr21:40981909-40981910	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570820261	chr21:40981917-40981918	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs111276817	chr21:40981933-40981934	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs553462927	chr21:40981934-40981935	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs565311895	chr21:40981949-40981950	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs377182065	chr21:40981962-40981963	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs571839051	chr21:40981965-40981966	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377660561	chr21:40981980-40981981	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs116422957	chr21:40981994-40981995	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544866412	chr21:40982000-40982001	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs564675765	chr21:40982004-40982005	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532934238	chr21:40982005-40982006	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs57304019	chr21:40982016-40982017	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs375713911	chr21:40982043-40982044	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528979884	chr21:40982083-40982084	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs548736117	chr21:40982088-40982089	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557055580	chr21:40982089-40982090	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs115684268	chr21:40982092-40982093	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531435832	chr21:40982100-40982101	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs377635112	chr21:40982108-40982109	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571458417	chr21:40982147-40982148	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs149742898	chr21:40982148-40982149	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs148312998	chr21:40982160-40982161	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553422174	chr21:40982180-40982181	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186925115	chr21:40982181-40982182	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs78916203	chr21:40982190-40982191	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs375524737	chr21:40982261-40982262	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555924468	chr21:40982338-40982339	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs575790167	chr21:40982381-40982382	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145672594	chr21:40982392-40982393	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs558390919	chr21:40982400-40982401	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs578189712	chr21:40982409-40982410	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs191302989	chr21:40982415-40982416	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559735442	chr21:40982428-40982429	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573338009	chr21:40982440-40982441	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554610520	chr21:40982452-40982453	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs35371707	chr21:40982480-40982481	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573077494	chr21:40982514-40982515	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Down syndrome	20877625	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21147910	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:393 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40970200-40982400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr21:40970400-40981800	Weak transcription	Pancreas	Pancrea
3	chr21:40970800-40984600	Weak transcription	Right Atrium	heart
4	chr21:40973400-40982400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr21:40974000-40982200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr21:40974400-40982200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr21:40974400-40982400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr21:40974400-40982600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr21:40976800-40983200	Weak transcription	Brain Anterior Caudate	brain
10	chr21:40977400-40982200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr21:40978200-40982000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr21:40980600-40982200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr21:40980800-40982400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr21:40981000-40981800	Strong transcription	H9 Cell Line	embryonic stem cell
15	chr21:40981000-40982000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr21:40981000-40982000	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr21:40981000-40983600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr21:40981400-40981800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr21:40981400-40982600	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr21:40981400-40982800	Enhancers	Duodenum Mucosa	Duodenum
21	chr21:40981400-40983200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr21:40981600-40982600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr21:40981600-40984200	Enhancers	Stomach Mucosa	stomach
24	chr21:40981800-40982200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr21:40981800-40982400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr21:40981800-40982400	Enhancers	Pancreas	Pancrea
27	chr21:40981800-40983400	Enhancers	Fetal Intestine Large	intestine
28	chr21:40982000-40982400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr21:40982000-40982400	Enhancers	Fetal Intestine Small	intestine
30	chr21:40982000-40982600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr21:40982000-40984200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr21:40982200-40982400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr21:40982200-40982400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr21:40982200-40982600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr21:40982200-40982600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr21:40982200-40982600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr21:40982200-40983000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
38	chr21:40982200-40983400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr21:40982200-40983400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr21:40982400-40982600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr21:40982400-40982600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr21:40982400-40982600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr21:40982400-40982600	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr21:40982400-40982800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr21:40982400-40982800	Flanking Active TSS	Pancreas	Pancrea
46	chr21:40982400-40983000	Enhancers	A549	lung
47	chr21:40982400-40983600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr21:40982400-40983600	Bivalent Enhancer	Fetal Intestine Small	intestine
49	chr21:40982400-40984200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr21:40982400-40984200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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