| Tag | Content |
|---|
EnhancerAtlas ID | HS180-51404 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chrX:147452650-147453960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chrX:147453595-147453607 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chrX:147453599-147453611 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chrX:147453603-147453615 | GTTTGTTTGTTT | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH0XI148372 | chrX | 147452841 | 147452990 | | GH0XI148371 | chrX | 147453048 | 147453533 |
|
Enhancer Sequence | ATTTAAGTGA TATATGATCA GGTTTAGGGT AGACAGGTTT AAGGATCTGC AAAAGGAACA 60
CCCAAAGAGA ATTGGGGGTG CCTGTGACAA ATCCAGCAGT TAGAAAGGGA TTCTCCTCTA 120
CTGATGATTT TGGAGAAGCT GACTAGGCTA TTGCGATTCC AGGGGCCTTG CACCCAGACT 180
AAAAGGAAGA GGGTATAATG AGAGCATGAT TAATATTCAA GGCAGGATGC CAGTTTGGTT 240
AATAATTATG CACTTGTAAG TGACTTGATT CTAGCCAATA GGGAGCAGAC AGAGTGATGT 300
CAACCAGTAG ATTATTAAGA AAACACTAAC AATTAACAGG AAGAGTAAGC ACACTCATAT 360
CAGTTATTTA TTTAAGAGTA TTGCTTAGTT TTATTGCTGC CTTCCAGAGG CAGCTTCCTG 420
AACAAATACT TGAGGTCCTC TGTAGGCTTC CCGGAGTAGA CTGTTTCCTC TGAAAAGGCC 480
TGTTCATCAG GAGAAGCAAA AGGTTTTATT CTAGAGACAT GGACTCAAGT CGGAAGTCCT 540
TCCAACGTTA TGACTGTTGG AGTGGACAAG ATAACCTGGT AAGGACCCTT CTATTTTTCA 600
GTTAACTGAT CCTCCGGGTT TCCTTCTCAC CAAGTCTTGA GTAGGACCTG TGAACCTGGG 660
CTAACACGGA AATGATCTGA AATCCCCTTT CCTAGCTGAG GTAATCTTAT TACTATATTG 720
AATGATTGAC TGCTGAACTC GTCCCAAGTT AATGATGTAT TTTAGAGCCT GATTTAAATC 780
TTCATCTAGC AGAAAGCTTG TTTTGAGAAA AGGCCACCCA CAGATCATTT CAAAGGGGTT 840
CAGCTTTATG TTTCCCTTTG GGACAGCTTT TAATCTTAGT AAGGCAATAG AAAGAAACTT 900
AATCTGTGAT TCCTTGGTGT TTTGGCATAG TTTAGCCAAG GTTTTGTTTG TTTGTTTGTT 960
TGTTTCTTAA AGAGTTTGGT TTATTCTTTC AACCTTCCTG GAATACTGAG AATGTCAGGT 1020
GGAGTGAAGT TTGTACTGGA TGCCAAGACT GCTAGACAGT CCTTGGGTGA CCCGGGTGAT 1080
AAAAGATGGC CTGTTGTCAC TTTGTAGGGA GGCTGAGAGC CTTAACCTAG GAATTATTTT 1140
TTTTAAGCAG CCATTTACAA ACTTTAGATA CTTTCTCTGT CCACATGGGA AAAGCTTTCC 1200
CCCAGCCTGT GAAAGTGTCT GCCAAAAATA AAAGATATTT GAATCCCCCT TTGGGAGCAT 1260
CTGTGAAAAA TCAGTTTGCA ATCCCCTCCA AGACAGGTCC CCCAGTGTTG 1310
|
