| Tag | Content |
|---|
EnhancerAtlas ID | HS048-39005 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chrX:129094710-129096050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chrX:129095374-129095384 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chrX:129095395-129095405 | GGGGCGGGGC | - | 6.02 | | SNAI2 | MA0745.2 | chrX:129094771-129094781 | AACAGGTGCA | + | 6.02 | | ZNF263 | MA0528.1 | chrX:129095084-129095105 | TCTTCCCTCCCCCTCTCCTCT | - | 7.15 |
|
| | 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 |
| GH0XI129960 | chrX | 129094751 | 129096176 |
|
Enhancer Sequence | TTATTTTCAT TTTAGAGACA GGGTCTTGCT ATGCTGCCCA GGCTGGAGGG CAGTGACTAT 60
TAACAGGTGC AATCATAGCA CAGTGCAGCC TCGAACTTGT TTTTCTGCTT CTTTTATACC 120
TCCAGAGCAC CTGATATAGG ACTGGCTCTG TACATGCTGG GCATTCCCAG GCCAGGGTAA 180
CCAGACAGAC CCATGATACA ACCTGCCAGC GAATCCCGGA AACTCCAGGA CAGGAGACAC 240
TTGCAGGCTA ATGGTGGTGT GCACCACCAG AGTCTTCGGC AGCTCACGGC CCTTCTATCT 300
GCCTTAAGTT GCTGGGGCAG AGAGCAGTGC CAAGGCAGAG AGGAAGGAGA ACATCCCTCC 360
GTGTAGACCC CAGCTCTTCC CTCCCCCTCT CCTCTGGGGC TTCAGCGGGT CCGGAGCTCA 420
TGAATAAAGC TAATATTGGA ACTAGTCGTA TACTAGTTGG AGAGGGGCTG TTGTCTAGAT 480
CCTCCCTTGC AGGGACGGGT TGTGCCAATA GAATGCCCCG AGGCCCCAGC CCTCTCGTGA 540
TGGTTGGCTG GAACTAAGGC ACCCCCCTCT CTCGCCCTTT TATGAGTCTC AGCTGATTTC 600
CCTGGAGGGC GGCCCCACTA GCCAGCGCCC CCAACCCGCT ACCGGACTCC CTCACTATAC 660
CTGGGCCCCG CCCCAACTGT CCTCAGGGGC GGGGCCAGCC CTAGGGCAAG CTGGGGCAGG 720
AAGTGGTTGC AATTACACAC ACTCCCGCCC CGCACTGGCT GCCACTGCCA GAGTGACAAT 780
GCTAACTCGG CCGGCCCCAA ACGTCAGGGC AAGGGCTAAG AAGAGGACTC AACCAGAGAA 840
GCTCCTGGGC TGGAACGAAG CTCTTTTCCT GAGAGAAGGG AGTTTCCGAG GTTAGGCTTG 900
GTTGGAAGCC TCAGCGGATT GTTGGTCACA TCCAGAGATG AAGGGAGGGG GTCGTGGGTC 960
TCCTTCCCCA CCCAGACATG GCAGTCACTC ACACCGTCAT CTCTTTTTAA CCTGGCCACT 1020
AGCTGACAGC AGCTTTTCCT AGCTGCTTGG GCCCCCTGCT CGCAACTGCC AAGACAGACA 1080
GCTCTGATCC CTCCTACCAG GGGAAGATGG GCTTTGATTC TCTACTACTG CAAACAACCA 1140
CAGCACAGTG GTTTCTATAT CCCCTACTCC TCCTTCGTTT CTTAGGCATT CCCATCTGGG 1200
GCGGCTCTGG GCCAGGTGGA GAGCGTGACT GGTATGGCCA CAGCTATGGG CTGAGAACCA 1260
TGTAGAGAGA GGGATGGATG GGGGAATTCG AGAATGTTTG GGTGGGATGA CTTCAGAACT 1320
CTCTGGGTTG GGCTTTCACT 1340
|
