Tag | Content |
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EnhancerAtlas ID | HS050-05011 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:183167270-183168220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:183167498-183167513 | TGACCTCCTGACCTC | - | 7.19 | RARA | MA0729.1 | chr1:183167495-183167513 | TCTTGACCTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_35834 | chr1:183165424-183170271 | HMEC | SE_64350 | chr1:183166735-183169409 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I183194 | chr1 | 183163373 | 183169370 |
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Enhancer Sequence | CTTTCTTTTT TTTTTTTTTT TAATTGAGAC AGAGTCTCAC TCTGTCGCCA GGCTGGAGTG 60 CAGTTTCGTG ATCTCGGCTT ACTGCAACCT CCACCTCCTG CGTTCAAGTG ATTCCCCTGC 120 CTCAGCCACC CCAGTAGCTG GAACTACAGG TGCCTGCCAC CACACCCGGC TAATTTTTTT 180 GTGTATTTTA GTAGAGACAG GGTTTCACCA TGTTGGCCAT GATGGTCTTG ACCTCCTGAC 240 CTCATGATCT GCCCGCCTTG GCCTCCCAAA GTGCTGGGAT TATAGGCGTG AGCCACCGTG 300 CCGGGCTGAG CATTATCTTT AAATGGTTCA TAGTTCGACT AATTCACGGG AGATTACAGG 360 TCACATCATA TAAACTTGCT GCTGTTTCAC TGAATCAGTT TTAGTGCACT AAGCAACCGA 420 AATGGTAGCA ACAGCAACAA AGCACTACGT AATAGCAACC AGCACACACT GTCAGGTTTA 480 AACATGATGC TCAAATTCCT AGCTCCTGAC ACCGTCCCAC ACAGCCGCCA AGTACACTAC 540 CTATCAAGGC TGCCTGAGCA CTGCAAACTG ATCTCATGCT CTGAGGCCTG CCTCATCGCC 600 TTGCCCTCCT CCCACACAGC CCTAGGCTCG CTGCCCGTTG AGGTGGCAGG CAGAAAGCAT 660 TGCAGCTCTG GGGTCATAGA CCACAGATGG GTGGGCAGTC CTAGGGTGGA AATAGTTCAT 720 CTGGTATGAG CAGCAACCTG AAAGTCCCAG ACCCTTAATC TCATTGAAAA TCTCATGTTC 780 CTCTCACAAT TCTTTCTGTT CCCATCTCAC CATGGATTTT TTTGCTTGGA ACATTAGTTT 840 TTTTACACTG AATGTCATAT ATGTAGACAA TGGAAACTTT GTGTAATGTA TTGGGGAAAT 900 TTGAAAGTAG GCTTCTGGAC GTCAGGGAGA TTTCTGTATG TTCAGGTTCT 950
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