| Tag | Content |
|---|
EnhancerAtlas ID | HS180-21656 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr17:73431800-73432810 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr17:73431804-73431819 | TGAACTCCTGACCTT | - | 6.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 73432401 | 73432536 | | chr17 | 73432149 | 73432392 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH17I075435 | chr17 | 73431681 | 73432644 |
| Enhancer Sequence | GTCTTGAACT CCTGACCTTG TGATCTGCCC ACCTAAGCCT CCCAAAGTGC TGGGGTTACA 60
GGCGTGAGCC ACTGAGCCCA GCTTTATTTA CTTTTTTTTT TTTGAGACTG AGTCTCACAC 120
TGTCGCCCAG GCTGGAGTAC AGTGGTGCGA TCTCAGCTCC CTGCAACCTC CACTTCCCAG 180
GTTCAAGCGA TTCTCCTGCC TCAGCCTTCT GAGTAGCCAG GATTACAGGC GTGTGCCACC 240
ACGCCCGGAT AATGTTTGTA TTTTTTTTAG TAGAGATGGG TTTTCACCAT GTTGGCCAGG 300
CTGGTCTCGA ACTCCTGACC TCAGATGATC CGCCCACCTT GGCCACCCAA AGTCTTGGGA 360
TTACAGGCAT GAGCCGCTGT GCCCAGCCTG TAAGCCACCA CGCCTGGCCC CAAGGAGTTA 420
TAAAGTTCAT TCGTTTCTAA ACCACACGCT AACCACACCC CATGATAAAA TCAAAACAAA 480
ACCAAGGCAA CAACTTGTGT CCCTCAGCCT TCTCTTCCTA GACAAACTGC TCAGCCACAG 540
GGTATCTCTT CCTGAGCACA AGAGGACTGC TTTCCCAGAG AGAGAGCATC TCCATTTATT 600
AGCTGACATC GCTTACAGTC ATTGCTGTGC CAACTCACCC CTGACCCCAT CCCCTCACCT 660
GGAGAAAGTG GCAAAAAGGA ATAGTGACAA CTTGGACATC TGACACCACC AACCTGGCAA 720
GGGACTGTCA AACGCTAAGC AGAGGCCAGG TGTGGTGGCT CACATCTGTA ATCCCAACAC 780
TTTGTGAGGC TAAGGTGGGC GGATCACCTG AGATCAGGAA TTGGAGACCA ACCTGGCCAA 840
AATGGCGAAA TCCCATCTCT ACTGAAAATA CAAAAATTAG CCAGGCACGG TGATGGGCAC 900
CTGTAGTCCC AGCTACTGGG GAGGCTGAGG AAAGGATCCT GGGCAAAAAG TTGCACGTGA 960
GCTGATACAA ACACATCACT CCCCTTACAC AAGGAGGAAT AACCATATGG 1010
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