| Tag | Content |
|---|
EnhancerAtlas ID | HS180-00256 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr1:9081540-9082970 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:9081543-9081561 | GTGAGGAAGCCAGGAAGG | + | 6.15 | | Gata1 | MA0035.3 | chr1:9082395-9082406 | TCCTTATCTGT | + | 6.14 | | Lhx3 | MA0135.1 | chr1:9082150-9082163 | AGATAATTAATTT | - | 6.64 | | POU6F1 | MA0628.1 | chr1:9082140-9082150 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr1:9082140-9082150 | ATTAATTAAT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCAGTGAGGA AGCCAGGAAG GCGAGGTTCT GGTGCCAAGA GCAGGGAGTG GGTGGTGAGG 60
ACTCTATGAA GATATCCCAG GTCGGCAACA CTGAGGACTG GCCAGGGAGT CCACAGACAA 120
GCAGGCTGGT GTTCTCAGGC CACTTTTCTC TCCCTGGGGC TGCCACAGCC TTCAGGAGCA 180
GCCACCAGAG CACATCCCCC ATCACGGGGA GGGTCAGCCA GCCAGGAGGC CCAAAAAGAC 240
TAAGCAGCCC CGACACGTTC CCACCCTTCT CTGGACTCCC AGCCCTTCCT GATGACTATA 300
AGGGGAGGCT GGGGCTGTCA GGACCCCACT GGGCAAGGCT GGCACCACCA CATTCCTGGA 360
CTCAGGCTCT TCATCTGGAA AATGGGTTCA GACAAGGAAG TGGAGGCCAA GACTGGGCTT 420
CCAGAACAGT CCAAACACTC TTGGTCTGGC TGAGAACATC ACAGTCTGGA TGACCAAAAA 480
AAAAAGCTTG AATTATGGTA TAGTTACATT AGAGTGAATT GTTTCTTCTT TCCAGCGCAT 540
AATGTATGGC AAATTAATTG TCGATCAAGT ATATGCAAGA AGAGGTCCTA TGAATCTTGC 600
ATTAATTAAT AGATAATTAA TTTTCAATCA GCGCTATTTT TTTCTATGCC TGAAAATGGA 660
ATTGCTCTGG TTTTTTGAGT GACTTTTCAC TAGAGGGCCT TCCAGTCACT CCTGCAAGCT 720
GTCTAACCTG GCACACCATG CCCAAGTGTA ACTGTGAGTC CGAATGAGTG GGCTGACCTA 780
AGGGAATGCC ACCAGGCCTC ATCCTGAGCC CAGGCTCACG CTTTGCCCTC CTGGGAACCT 840
TGGCCTGTGC ATCTTTCCTT ATCTGTGGAG TCACGTCTTT GGAGCACCTG GGCTTAGGAA 900
GAATGATTAG TGAATCTGTG TAAGCCAAGC AAAGTTCAAA GACCTGCCCA GTCTTCATTT 960
CCAAATAATC TCGTATCTAT GAGACAGTGG CCGGCAGCGT GACTCAGCCT GACCCCAGCC 1020
TCAGTAACAA ACTCTGGCAA AGACACGCGG GGAGAGGCTG CAGCGCTTAG AACTTGGAGC 1080
CATGGTCACC TGACCCCGGA ATGAAACCTG ATAAACGAGC ATTTACTGAA CACCCACTGG 1140
AAGTGCTTAC AAGGCACTAA GCTAAGCACC GTCAAGAACC TTGATCTCAA AGGCTGCACC 1200
ACCTCTGTGG CAGGTGACGG AAGGGAATGC TTTTCCCATG CAACTACCTA GGAAAGAAAT 1260
CCCAGAGACA TTTAGGGACT GGTTTAAGGT CATGATGACT GTGGCCAAGC GGAGACTAGA 1320
CTTCAGATCT CCTGATTTTC AGGGTCACAC GTCTCCCCAC CAGGTGCACA AATGCCCAGA 1380
GACAGTGTGG CTTACTAGCA TGAATTTTAA GTGGGAGCAG TGCACCTTCT 1430
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