| Tag | Content |
|---|
EnhancerAtlas ID | HS180-48530 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr9:4422070-4423520 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr9:4422763-4422774 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr9:4422764-4422774 | GGGGCGGGGC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATTTCTCAAA AAGTCAATTG TGTCCATCAC CGCTCAAGAA TTATGGTAGG TTTAAATCTT 60
CCACCAGATT TTGTGTTAAT GAAAAAGCAC ATATGTAACC ATATCATAAA TTTGTATTTC 120
AACACTTTGA TGATTGTATT TCAGTATAAT TGGTCTTCTT CATAATCCTA TGTGTTTTAT 180
TTTATGCATT GTTCTGAGAA AGAGTCCATA GGCCTCATCA GATAACAAAG CAAACCTTGG 240
CACAAAATGA TTATGAATCC TTGTCCTAGT AAGACAGACA GGCCTTAAAT AAATAATCTT 300
ACAAATACAT ACTTACAGAC AGTGCTAAGA TCTCTAAAGA AAAAGTCCAT GTATGTGAGA 360
TGATAAAAAG AAGACATGGT TTCCCCAGGA TTTGGGGTTA GTGGGCTACC CCCAGGAGTC 420
TAGTGGGATC CACCTGGATT CTGTTTCCCC TGGAAAATAT CACATTCTGC TGCAGTCAAC 480
CAGTCCATAA AAAATATCAG TTACATATCT CTCCTGTGCT AGGTCCTATA TGAGCACTGG 540
GGACACAACA TCTCTGCCTG CCAGTCTACC GGGGGAAGTC AGAGCAAACC ACACATGAGG 600
AAATACAAAT CTCAGATAAG CTCAGTTAGA GATCAGAGCC CTGAAGAAAG TGAAGCAGGT 660
TAATGAGATA AAGTGTGAAA GTCAGGGAGT GCTGGGGGCG GGGCAGCCCA GGGAAGGTCT 720
CTTGCAGAGG TGATATTTGC ACTGAGACCT AGAGGAAGAG ATTTGGGGGA TACATTTAAG 780
ACACAAGGCA AAGACCCTGA GATAGAAAAA GTAAACCCTC AGTTCCTTTG AACCCCAGGA 840
CCCAGACTTC TTAAACAGTG GTCATTGTTG CCTTGCTATG CCCTGTTTTT GGAGAAAGAA 900
GCACATCACA GGAGTCAAAA GAGAAAATTA GGTGTGTTCT AAGGGTCAGG TGGACAGAAG 960
GGGTCAGAAG CAGCAGTGGG GACATGGATC GAGTGCCTGA GTATATGCCT CCATAGGTGG 1020
GGTCCCCTGA AAAAGGTCAG GGGACCCTCC CTACCTCTGG GCAACTCCGA TCATTTCCCA 1080
GCCCAGTTCA TCACCATCTG CCTTTTAAAC AACAAGTGCC GATTATCAGA GAACCTCCTC 1140
AGGTCTGGAG AGGATCCACA AATATTTGTC ATCTGACGTC ACAGACCCCA AGACCCCTAA 1200
TTTTCAGGGA GCTGAAGCTG AAACTAAACT CCACCACACG GAAGGGCGGC TATTTCCCTC 1260
TGAGTTGCAT CTTAGTCTTA GCTCCCAAGG CCTCCTGGTG GGCACAAGAG TTCTACTCAA 1320
CCCATCTTTT CCCAGCTGGA TCCAGAGAAA GCTACTCATT CCCCCAACTT CCCACACCCC 1380
TCCCCCAGAC CTTTAGAAAA ACCACTCTCT TTCCCAATGA AAAATGACAC CAAAGCTCCT 1440
ATCTGGCAGC 1450
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