| Tag | Content |
|---|
EnhancerAtlas ID | HS050-69114 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:90124300-90125540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr9:90124493-90124508 | TGAACTCCTGACCTT | - | 6.04 | | TFAP2A | MA0003.3 | chr9:90124976-90124987 | AGCCTCAGGCA | + | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_13792 | chr9:90124488-90126581 | CD34_Primary_RO01536 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I087509 | chr9 | 90124026 | 90126325 |
|
Enhancer Sequence | AGTTTTCCTC TTGTTGCTCA GGCTGGAGTG CAATGGCGCA ATCTCAGCTC ACCACAACCT 60
CTGCCTCCGG GTTCAAGCGA TTCTCCTGCC TCAGCCCCCC GAGTAGCTGG GATTACAGGC 120
ATGCACCACC ACGCCCCGCT AATTTTATAT TTTTAGTAGA GATGGGGTTT CTCCATGTTG 180
GTCAGGCTGG TCTTGAACTC CTGACCTTAG GTGATCCGCC CGCCTCGGCC CCCCACAATG 240
CTGGGATTAC AGGCGTGAGC CACCGCGCCC GGCCATCCTG CCAGCGTTTT CTTCTGTGCA 300
CTTGGGATGG GAATATAGAA AATTGTCTTC CTAGATATTG GCTTTGCCAT TCAAAGTCTC 360
TACAGTCAGT GTGTGAACTG CTGGGAGTGA TGCCAGAATC TTTCACAGAT TTCATTCCTG 420
GGAGCTCTTC TGGCGTCAGA TGATCGCGGT TTCTTTTCCT TCTGCACCAC AGCACATGGA 480
GGAGGCCTCT TTCTCACTTG CTCCGTTCCT TTGCCATTCA TGGAGGCAGT GGCACCAGTG 540
AGCTCACGGC CAGGCCGCTT TTGCCCTTTT TCTGACTAAG TCACTATAGA TGGACTAAAC 600
AGAATATATT TACAGTTCGC CCATTTAGAA TCGATAAGGG TGTGCCCCAG GCTCCATCGT 660
ATATTCCATT ACATACAGCC TCAGGCATCC GTTTCAATTG TTTGGGAGAG GAAGTGAATT 720
AGCACAAGTG GAATATCTAC AGGATGAAAC GTTGTCAGTC TGTGCGTTCC TCCCCACCCC 780
TTCGTTGGCT GGAAGAGATA ACGCTTGACA CGTATGGAGC AGACAGGGTA ATGTCAGCCT 840
CGTGGCCATG GAGAAGCAGG AAGTCCCTTG GTTTTGTTCA GTGTGATTTG GGCATTGAAT 900
GAGTAGATCC TGTTTTAAGA ATATTACTCA TTAATATGAA CCATCATTTT GTAGGTCTTT 960
TAGAAGCAAC ATTCTCTTTA GTGCAGATAA TGCTTATCTG CATTGAGAGA AGTTATAATA 1020
ACCTGGAGAA TGAGAAGGAA ATACACATGC GAAATGGCCC AGCCGGTTTC TCCTGGCAAC 1080
CTCTCCAGAG CATGTCCTAG GCTACTCCTC CAGGAAGGCT CCTGCTCTGA TTTCCTGTAT 1140
TCCTTCACGA TTTGGAGTAG ATAACTGGCC ACTTGGCATT CTTATTACAG GGGACTTATG 1200
CGTGGGATTA TTGGCTTCCC CTGTGGACTG TGAGTTTTCT 1240
|
