Variant report

Variant	esv20340
Chromosome Location	chr21:40814284-40816976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:35)
CpG islands
(count:123)
Chromatin interactive
region (count:31)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:35 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:40816702-40816848	HepG2	liver:	n/a	n/a
2	BRCA1	chr21:40816496-40817143	Hela-S3	cervix:	n/a	n/a
3	CHD2	chr21:40816468-40816662	K562	blood:	n/a	n/a
4	CTCF	chr21:40816600-40816750	HCPEpiC	choroid plexus:	n/a	n/a
5	CTCF	chr21:40815160-40815310	GM12873	blood:	n/a	n/a
6	CTCF	chr21:40814380-40814530	GM12864	blood:	n/a	n/a
7	CTCF	chr21:40814220-40814370	K562	blood:	n/a	n/a
8	CTCF	chr21:40815520-40815670	Caco-2	colon:	n/a	n/a
9	CTCF	chr21:40814140-40814290	HEK293	kidney:	n/a	n/a
10	CTCF	chr21:40814340-40814490	GM12873	blood:	n/a	n/a
11	CTCF	chr21:40814220-40814370	HPF	lung:	n/a	n/a
12	E2F4	chr21:40816705-40816815	MCF10A-Er-Src	breast:	n/a	n/a
13	GATA2	chr21:40816678-40817858	SH-SY5Y	brain:	n/a	chr21:40817179-40817187
14	GATA3	chr21:40816974-40817303	T-47D	breast:	n/a	chr21:40817179-40817187
15	HCFC1	chr21:40816914-40818182	K562	blood:	n/a	n/a
16	MAZ	chr21:40816767-40818164	IMR90	lung:	n/a	chr21:40817927-40817936
17	MAZ	chr21:40816716-40816847	Hela-S3	cervix:	n/a	n/a
18	MXI1	chr21:40816468-40818248	IMR90	lung:	n/a	n/a
19	MXI1	chr21:40816307-40818898	SK-N-SH	brain:	n/a	n/a
20	MYC	chr21:40816901-40818552	K562	blood:	n/a	chr21:40817927-40817936
21	POLR2A	chr21:40816294-40816549	K562	blood:	n/a	n/a
22	POLR2A	chr21:40816742-40816921	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr21:40816598-40818147	IMR90	lung:	n/a	n/a
24	POLR2A	chr21:40816944-40817136	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr21:40816939-40817109	ProgFib	skin:	n/a	n/a
26	RCOR1	chr21:40816457-40816895	K562	blood:	n/a	n/a
27	RCOR1	chr21:40816543-40816649	K562	blood:	n/a	n/a
28	REST	chr21:40816476-40818393	H1-neurons	neurons:	n/a	n/a
29	RFX5	chr21:40816419-40816424	K562	blood:	n/a	n/a
30	SIN3AK20	chr21:40816478-40818410	MCF-7	breast:	n/a	n/a
31	SIN3AK20	chr21:40816970-40818280	MCF-7	breast:	n/a	n/a
32	SMARCC1	chr21:40816551-40818214	Hela-S3	cervix:	n/a	n/a
33	TEAD4	chr21:40816477-40818634	K562	blood:	n/a	n/a
34	ZMIZ1	chr21:40816571-40816624	K562	blood:	n/a	n/a
35	ZNF384	chr21:40815936-40816028	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:40816035-40816085	MCF-7	breast:	n/a
2	chr21:40816035-40816085	MCF-7	breast:	n/a
3	chr21:40816035-40816085	SK-N-SH_RA	brain:	n/a
4	chr21:40816035-40816085	AG04450	lung:	fetal
5	chr21:40816464-40816514	PANC-1	pancreas:	n/a
6	chr21:40816464-40816514	GM12891	blood:	n/a
7	chr21:40816464-40816514	GM06990	blood:	n/a
8	chr21:40816464-40816514	HCM	heart:	n/a
9	chr21:40816464-40816514	NHBE	bronchial:	n/a
10	chr21:40816464-40816514	IMR90	lung:	fetal
11	chr21:40816464-40816514	LNCaP	prostate:	n/a
12	chr21:40816464-40816514	AG04450	lung:	fetal
13	chr21:40816035-40816085	AG04449	skin:	fetal
14	chr21:40816464-40816514	K562	blood:	n/a
15	chr21:40816464-40816514	MCF10A-Er-Src	breast:	n/a
16	chr21:40816464-40816514	HIPEpiC	eye:	n/a
17	chr21:40816464-40816514	Hepatocyte	liver:	n/a
18	chr21:40816035-40816085	HIPEpiC	eye:	n/a
19	chr21:40816464-40816514	SKMC	muscle:	n/a
20	chr21:40816464-40816514	A549	lung:	n/a
21	chr21:40816464-40816514	HNPCEpiC	eye:	n/a
22	chr21:40816464-40816514	SK-N-SH	brain:	n/a
23	chr21:40816035-40816085	Hela-S3	cervix:	n/a
24	chr21:40816464-40816514	HL-60	blood:	n/a
25	chr21:40816464-40816514	AG10803	skin:	n/a
26	chr21:40816035-40816085	HEK293	kidney:	embryo
27	chr21:40816464-40816514	Hela-S3	cervix:	n/a
28	chr21:40816464-40816514	HRCEpiC	kidney:	n/a
29	chr21:40816464-40816514	SAEC	small airway:	n/a
30	chr21:40816464-40816514	Jurkat	blood:	n/a
31	chr21:40816035-40816085	RPTEC	kidney:	n/a
32	chr21:40816035-40816085	NHBE	bronchial:	n/a
33	chr21:40816035-40816085	HAEpiC	amniotic membrane:	n/a
34	chr21:40816035-40816085	A549	lung:	n/a
35	chr21:40816035-40816085	HepG2	liver:	n/a
36	chr21:40816035-40816085	HRCEpiC	kidney:	n/a
37	chr21:40816035-40816085	HL-60	blood:	n/a
38	chr21:40816464-40816514	HEK293	kidney:	embryo
39	chr21:40816035-40816085	HMEC	breast:	n/a
40	chr21:40816035-40816085	ECC-1	luminal epithelium:	n/a
41	chr21:40816035-40816085	HNPCEpiC	eye:	n/a
42	chr21:40816464-40816514	U87	brain:	n/a
43	chr21:40816464-40816514	HRPEpiC	eye:	n/a
44	chr21:40816464-40816514	SK-N-MC	brain:	n/a
45	chr21:40816464-40816514	Caco-2	colon:	n/a
46	chr21:40816035-40816085	CMK	blood:	n/a
47	chr21:40816035-40816085	HRE	kidney:	n/a
48	chr21:40816035-40816085	Caco-2	colon:	n/a
49	chr21:40816464-40816514	AG09319	gingival:	n/a
50	chr21:40816035-40816085	AoSMC	blood vessel:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:40812406..40815051-chr21:40815498..40817690,4	K562	blood:
2	chr21:40782804..40784995-chr21:40816330..40818172,2	K562	blood:
3	chr21:40750443..40753981-chr21:40814998..40818130,3	MCF-7	breast:
4	chr21:40758092..40760884-chr21:40816362..40818206,3	K562	blood:
5	chr21:40554820..40556384-chr21:40814358..40816122,2	MCF-7	breast:
6	chr21:40719410..40723060-chr21:40814028..40819084,9	K562	blood:
7	chr21:40552682..40557091-chr21:40814575..40819975,14	K562	blood:
8	chr21:40683837..40687545-chr21:40816624..40819639,6	K562	blood:
9	chr21:40683646..40687466-chr21:40813293..40816602,5	MCF-7	breast:
10	chr21:40684107..40685647-chr21:40816624..40819498,2	K562	blood:
11	21:40748850-40752541..21:40812812-40815481	K562	blood:
12	chr21:40719238..40723494-chr21:40813785..40819496,7	MCF-7	breast:
13	chr21:40553201..40555417-chr21:40813842..40815672,2	MCF-7	breast:
14	chr21:40791594..40793834-chr21:40813541..40816112,2	K562	blood:
15	chr21:40553976..40556398-chr21:40816228..40819085,2	MCF-7	breast:
16	chr21:40685795..40687913-chr21:40812651..40815254,2	K562	blood:
17	chr21:40759156..40760884-chr21:40816362..40818324,3	K562	blood:
18	chr21:40757952..40760815-chr21:40812863..40817486,4	MCF-7	breast:
19	chr21:40555615..40557158-chr21:40816762..40818748,2	MCF-7	breast:
20	chr21:40719979..40722729-chr21:40816056..40819504,5	MCF-7	breast:
21	chr21:40816254..40817919-chr21:40832845..40834906,2	MCF-7	breast:
22	chr21:40683731..40685549-chr21:40816150..40817682,2	MCF-7	breast:
23	chr21:40808329..40812009-chr21:40812185..40815067,5	K562	blood:
24	chr21:40552682..40557546-chr21:40815502..40820280,12	K562	blood:
25	chr21:40808402..40815127-chr21:40815513..40821149,12	K562	blood:
26	chr21:40570372..40572709-chr21:40816957..40818525,2	MCF-7	breast:
27	chr21:40758008..40760801-chr21:40816074..40819285,3	MCF-7	breast:
28	chr21:40719600..40723122-chr21:40811701..40815528,3	K562	blood:
29	chr21:40759083..40761929-chr21:40813666..40815597,2	K562	blood:
30	chr21:40720623..40723017-chr21:40815562..40818761,4	K562	blood:
31	chr21:40808402..40815127-chr21:40815513..40821149,12	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGN1-3	chr21:40816061-40816127	NONHSAT082192
2	lnc-HMGN1-3	chr21:40815385-40816127	NONHSAT082195

No data

Variant related genes	Relation type
LCA5L	TF binding region
SH3BGR	TF binding region
LCA5L	CpG island
SH3BGR	CpG island
ENSG00000183527	chromatin interactions
ENSG00000255568	chromatin interactions
ENSG00000205581	chromatin interactions
ENSG00000238141	chromatin interactions
ENSG00000182093	chromatin interactions
ENSG00000185437	chromatin interactions
ENSG00000272991	chromatin interactions
ENSG00000227406	chromatin interactions
ENSG00000185658	chromatin interactions
ENSG00000157578	chromatin interactions

Extended variants
information (count: 121 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:121 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558568163	chr21:40814288-40814289	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs147247179	chr21:40814294-40814295	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs531126825	chr21:40814298-40814299	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs58900137	chr21:40814326-40814327	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs564732978	chr21:40814356-40814357	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs113342111	chr21:40814376-40814377	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs562673512	chr21:40814395-40814396	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs547115206	chr21:40814410-40814411	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs529875827	chr21:40814442-40814443	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs566847404	chr21:40814482-40814483	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs570460410	chr21:40814489-40814490	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs549406182	chr21:40814512-40814513	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs376277277	chr21:40814545-40814546	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs56866897	chr21:40814605-40814606	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs556953468	chr21:40814666-40814667	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs577002232	chr21:40814677-40814678	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs539247336	chr21:40814699-40814700	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs181145677	chr21:40814713-40814714	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs572613677	chr21:40814792-40814793	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs561406084	chr21:40814793-40814794	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs144451091	chr21:40814802-40814803	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs541492107	chr21:40814807-40814808	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs149751803	chr21:40814816-40814817	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs145549171	chr21:40814827-40814828	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs184254010	chr21:40814837-40814838	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs148451797	chr21:40814857-40814858	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs533624084	chr21:40814860-40814861	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs564932598	chr21:40814866-40814867	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs61154033	chr21:40814876-40814877	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs560625661	chr21:40814878-40814879	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs532827503	chr21:40814883-40814884	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs146453228	chr21:40814896-40814897	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs377109223	chr21:40814926-40814927	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs140947895	chr21:40814972-40814973	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs144571766	chr21:40814973-40814974	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs538226012	chr21:40814988-40814989	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs188207339	chr21:40815006-40815007	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs180997469	chr21:40815015-40815016	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs539680197	chr21:40815090-40815091	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs146666760	chr21:40815095-40815096	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs566304758	chr21:40815102-40815103	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs369879751	chr21:40815132-40815133	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs535202165	chr21:40815153-40815154	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs186412651	chr21:40815154-40815155	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs574938178	chr21:40815168-40815169	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs73367979	chr21:40815176-40815177	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs536825241	chr21:40815199-40815200	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs114150314	chr21:40815239-40815240	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs578192433	chr21:40815274-40815275	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs540886047	chr21:40815285-40815286	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40778200-40816600	Weak transcription	Pancreas	Pancrea
2	chr21:40778400-40816600	Weak transcription	Left Ventricle	heart
3	chr21:40802600-40816200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr21:40802600-40816600	Weak transcription	Right Atrium	heart
5	chr21:40809400-40816400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr21:40809800-40816600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr21:40811600-40816600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr21:40812600-40816600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr21:40813000-40814800	Enhancers	HSMM	muscle
10	chr21:40813000-40815400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr21:40813400-40816400	Weak transcription	Hela-S3	cervix
12	chr21:40813600-40814400	Enhancers	Fetal Kidney	kidney
13	chr21:40813600-40814600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr21:40813800-40814400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr21:40813800-40814600	Enhancers	HMEC	breast
16	chr21:40813800-40814600	Enhancers	K562	blood
17	chr21:40813800-40814800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr21:40813800-40816600	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr21:40813800-40816600	Enhancers	Fetal Heart	heart
20	chr21:40814000-40814400	Enhancers	H1 Cell Line	embryonic stem cell
21	chr21:40814000-40814400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr21:40814000-40814400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr21:40814000-40814400	Enhancers	HSMMtube	muscle
24	chr21:40814000-40815000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr21:40814000-40815000	Enhancers	Fetal Muscle Leg	muscle
26	chr21:40814000-40816600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr21:40814000-40816600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr21:40814000-40816600	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr21:40814000-40816600	Weak transcription	Right Ventricle	heart
30	chr21:40814200-40814400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr21:40814200-40814400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr21:40814200-40814400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr21:40814200-40814400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr21:40814200-40814400	Bivalent Enhancer	Placenta	Placenta
35	chr21:40814200-40814600	Enhancers	Fetal Muscle Trunk	muscle
36	chr21:40814200-40814800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr21:40814400-40814600	Flanking Active TSS	Fetal Kidney	kidney
38	chr21:40814400-40814600	Enhancers	Ovary	ovary
39	chr21:40814400-40814800	Flanking Active TSS	HSMMtube	muscle
40	chr21:40814400-40815000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr21:40814400-40816000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr21:40814400-40816600	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr21:40814400-40816600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr21:40814600-40814800	Enhancers	Fetal Kidney	kidney
45	chr21:40814600-40815000	Weak transcription	K562	blood
46	chr21:40814600-40816400	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr21:40814600-40816600	Weak transcription	Fetal Muscle Trunk	muscle
48	chr21:40814600-40816600	Weak transcription	HMEC	breast
49	chr21:40814600-40816800	Weak transcription	Ovary	ovary
50	chr21:40814800-40815000	Flanking Active TSS	Fetal Kidney	kidney

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