| Tag | Content |
|---|
EnhancerAtlas ID | HS180-45367 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr7:97792550-97793880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr7:97792746-97792757 | TCAAGGTCATA | + | 6.62 | | Esrra | MA0592.2 | chr7:97792745-97792756 | GTCAAGGTCAT | + | 6.32 | | Esrrg | MA0643.1 | chr7:97792746-97792756 | TCAAGGTCAT | + | 6.02 | | KLF5 | MA0599.1 | chr7:97793690-97793700 | GCCCCGCCCC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 97792653 | 97792940 | | chr7 | 97792998 | 97793841 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I098163 | chr7 | 97792433 | 97794706 |
|
Enhancer Sequence | CTCTGGAATT GTAAAGTTAG ACGTGGTTAC AATGCCAAAT GGTATTTTAT GCATTTTTTT 60
TTACCCCAGT AGAAAAAAAT GGATAATTAC CTCCCACAAT TTAAGGTGCC ATGTCAGGTG 120
CTACCTATGT TCGGAGGCTA GGATGCCCTT TGGAAATCTT TGGTTATCAC TTGGCGTGGC 180
CAGTCATATA TCAGAGTCAA GGTCATAAAC ACAGGGTGCC ACCAACTTGT CCAGCAGTGG 240
GAGGTCACAT TGTTTCCTTG GGCAATTTCG TACATATCAC TTCTGGGCTC TCGTAAACTT 300
GAAAAGGAAC AGGTTTTCCA GCAGCAAGGA CTAGGGGCCT GACAGGGTTC TTGGCACTGA 360
AGTCCAGCTT CTCCGGGCTC CCACCGTGTG GCAAGAACGG TCAGGTAGCA CCAGCCCAGG 420
GAGCCAGAGA GGGCATCTAC TTGAAGGGAC CGAGGGTTGT CCCATGGGAC ACACCAAAGT 480
GTCTCTTTGA CACTGAGCCC AGCTCCCAGC CTGGATGACC CAAAACCTGC CCAGAAACAG 540
GCCTTTCTGA TCAGAGGGGC ATAACCCAAG GCAGGACCTG CCCCCTGGCC GCAATACAAA 600
GGGCACAAAG GGCACAGAGG GCAGCGGTCT GGGCTCTGTA AAAAGCTGCT GTGGCCACGG 660
TGAAGGACCG GCTATCGCTG CCTGTCTTAG CAGGTCAAGA GCGATTGAAT GAACAGTGGC 720
CTTTTCAGTC GTCATCCTGC AGTCATCATG CCCAATGATA ACATCTCCCA AGTAGAAAGG 780
AGAAAATATT TTTGCACTTA CTTAATTCCT TGTAAGATGG AATTAACCAG CCTGTTTTTA 840
AAAGGCACTT AATCATGGAA TTTTTATGAA AGTAAATGAA AACTCCTCTG AGTGCATTTT 900
GTAGCTGGCC TGCAGCCACA GATTTGCAAT GCTGACGGTG ACAATGTTTA TGAGAGGAGC 960
CGAGAGATGA CTGTAGGGTG TTTTATAGAA CTTGTTGCCA TGGCAGGTAC ACGCCGCTCT 1020
CACGTGAATA TCAAGGCAAT GAGACTTTTG ATTAAGGATC ACTCACTCAA CAAAAATGGA 1080
TTGAGCAAAT TCGAAGTGCC GGGAGCTGCC TGGTGCTTTA AGGAACACAG AAGTGAATAA 1140
GCCCCGCCCC TGACTTGCCT GCTCGGATGT TCATTCTGCC ACTCACTGGT TTATCACCTT 1200
GGAAAATCCC TTAACCTCTT CTGTAAAATG GCAGTAATAC TGTCTCCCCT TAGAACTGCC 1260
CTGACCATTA AGTAAGATGA TGGATGAGAT TACCGAGCAC AAGGAAAATG CTCAGTAAGT 1320
GGTGGCCATT 1330
|
