| Tag | Content |
|---|
EnhancerAtlas ID | HS180-00556 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr1:17058600-17060060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Tcf12 | MA0521.1 | chr1:17059893-17059904 | CAGCAGCTGTT | - | 6.32 |
| | | 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 |
| GH01I016732 | chr1 | 17058895 | 17059496 |
| Enhancer Sequence | TTTATAAATT TAGAAGGGAG ATTTTATTTT TTATAAATGG TTACAGCCTG CAAGGTGGCC 60
ATTCTGACAG ACAGGGAGGC ATACCCTCTT GCTGCTGAAA CCTGAAAAGT ACGTTTCCAG 120
GGAGGGGAGG GGGGAACAGG GATTTATGTT GATGTGGTGG GCCACATATA CATATTCAAC 180
AGGGAATAGG AGGAGCTCTG AATATTCATG AAGGGATCCT GCTGCATGCA TGCTGAGTAA 240
ACATGCCTGT TACATGCAAC CCATGTTCAT TTTGGGGTGG AGACAACATT TAAATACATT 300
ATAATTAGGC CCTATGCTTC AAAAGGGGAA GCAGGGACAC AAAGGCAGTC AAGTGCACAG 360
CCTCTGTAAA CCGTCCAGAA CCCGTCCACA GCCAGTGCTC TCTTATCAAG GGGAAGTTAC 420
TGAAATCAGT CTCTTGTCCA ATCAAAGCTG TAGTTATGGC TTGTGTAGGG AGGGCTCAGT 480
CAGTTTATGG TAATGGGTGA GCTGCAAGTG CTTCAGCATT GCTTATCTCA AGGCCAGTGC 540
TTGTTTAGCT AGAGAAAAAA AGGAAGAAGA AAAAAACCTG TGGCAATTGG AACATAGTTT 600
ATTCTTTAAG TTGAGGGGCG CATGACTCCA CCTTGCCTGG CGTGGCCTTA GGTCTCGTTT 660
ATCATACCAT ATCTTACTAC TGCAAGGAGT CTGTTCTGTC AGTCTTAGGA TCTCTATTTT 720
AACAATAATG CTGGTCAGTT GTGTCTAAAC CACAAAGGGA GAGAGTATAA GGAGAGGTGT 780
CTGAGATTCC AACTACTGGG CAGGAACTCA GTAGTTAAGA CTTCTCTGGG GTCTCCTTGG 840
CCAAGAAACA GTCTGTCCAG TTGGTTGAGT GGCTTTGGAT TTTAATTTTA GTTCTCAAAG 900
CATTTAATTT GATGAAATTT TGCCATATTT TTTCTTTATT TTTAAAGCCT GTTATGTTCT 960
ATAAGAAATC TTTCTACTCA GGATAGTGAA TGTATTCTCT TAATTTTATC TCTCTATGAG 1020
TTCCAGCGTT TTAGTTTTAA TTTTTAAATT GATGACATCT AAAATTCTAC TCCTAACCAA 1080
AACATTCCTG GGGGTGACCA AGGACAACTC CAAAAATCTT CCATAAATGG AAGTAAGACT 1140
TACTCCTTGA AGAACTTACT GGGATCTGGG CCTGCAGGGC ACAGTGGCTT TAGTGCACCT 1200
CTGCTCTTAC GACTATTCAG AAATTGTCTT TGTGAACCCA TCAGGCTGTT TCAAAATCAG 1260
CAATTTAGGG CTTGCTTGCA ACATGCAGTT ATGCAGCAGC TGTTTTGTGG ATCTGGTGAG 1320
TGCCTGCACG CATAGTTCCC CGGGAATTTT CTGAATTTGA ATTCTCATGG TATTTCAAGT 1380
GGCTCAGTTG TCTCTTTCTT TTCTTTTCTT TTCTTTTCTT TTCTTTTTTT TTTTTTGAGT 1440
CAGAGTCTTG CTCTGTCACC 1460
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