| Tag | Content |
|---|
EnhancerAtlas ID | HS050-18403 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr13:36604700-36606180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr13:36606090-36606111 | GAAGGAGAAGAGAAAAAAGGG | + | 6.06 |
| | | 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 |
| GH13I036030 | chr13 | 36604728 | 36605870 |
| Enhancer Sequence | ACCAAAGTGC TGGGATTACA GGCGTGAGCC ACCATGCCTG ACCCATTTCT TTTTAACACA 60
CTGAGTCTGG ATAGTACTTG ACCATTAGGG AACAGTATCT TCATTATTCA AATTTGGGGA 120
CAGTACATTA CTAAAAATAA ATATTATACT CAAAGCAAAC TTTTTCAACA GAGAAAAGTT 180
ATCGATATAG GGCACAGAAC AAATAGAATA AACGTTTCTC AGGTTTTTTG CCTGCAGCAG 240
AGAGGCAGGT CCCAGGGAAT CTCCCCAACT GATCAGCTCC CATCCCATTC ACTCATTGCT 300
GTGCTCTCAC CAAGCCACAC TTCCCACAAT GCCGGCCCAG CACCTTGTTA TTTCAGACCT 360
CTGCGTCTTG GGAGGCATTG TTCCCTTAGC AACTCGAAGA AAGAACATTG CCCTGTGTTC 420
TGCAGGTATA ACTGATAAGC CACAGGACTT ATTTCTAAAC CATGTATAAG ATGACACAAA 480
ACAGTCCTCA CTCCTACGCT TTTCCCAGCA CCACAGTGAT TGCTCAGACT CCGTCTCTGG 540
AGTTTCAGCC CTTCACAGCC TGGGCCCATT TCCTCAAAAA CCCGAAATAG TGGTGAGTCA 600
TCATCCTTTG AATCTGGATT TGACTTTGGA AAATAGCCAA AATCAAATTA GCAAATAATG 660
TGTGTGATCA AACTGGATAA TTCCATTTAG GCTAAAAAGT TTTAAGCACA AAAGAGTGAT 720
TTTTCTTGTG AGGCTCATGG ACTGGGTCCA ATATCAACCA CACACACACA AAAAAAGACG 780
AGCTTCAAAA GTATTTTGCT TTTCTATAAC ACGGCTCCAA GTAGCTTGAA CTCTGCAGTG 840
GTAATGGTGT CAAAGGATTG GGGTTTATTT AGATATATAT GTACACAAAT TATATGTACG 900
TACATATATA TGTGTGTATG TGTTCGTACA TATGTCATCA AATGCGATTT TAAAAGATCA 960
GTCCTGTGAT TTTATTGCCA GCAGGCCTTA AATTATTTCC TGGTAATACG TTTGACAATA 1020
TAAAAAGGTT CCTTATTCTT ATTAGATAAT TAAGTACCAT TTGTTAAGTT GTAAAGATGA 1080
ATTTTGACAT CCTCAGTATT ATTTACAGTG ACGTATTTGA TGACTTCCTG GGAGGCTGCT 1140
GGTAAGTGGT TAGTGTAAAA TGGAATAGCA TGGTCTTCTG ATCCCCTATG CGATTTGTTG 1200
TGGTTGTTGT TGAAACGCGT GGCTGTCATG TCAGCGCAGG AGGAACTGCT TTGCACGTGG 1260
CTTCTACACA GCTGGCTGCT GTTTGCATCT GACTGAACCT CCCACCCAGA TCCCTGCTAG 1320
GCCCCACCTG ATAGACGTGA GGTCTCAGCA GTGGAGGTCA GACTGGATGT GCAGCTCAAC 1380
ACTTTAGGTG GAAGGAGAAG AGAAAAAAGG GAAGGGGACA GGTCTGTGGG GCAGGCCCCT 1440
TTTAAACCAT TCATTAATCT TTCTTTCACT CCCCTGGGTG 1480
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