| Tag | Content |
|---|
EnhancerAtlas ID | HS108-42878 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chrX:129094730-129096240 |
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 | | Nr2f6(var.2) | MA0728.1 | chrX:129096212-129096227 | GAGGTCAGGAGTTCA | + | 6.22 | | 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 | GGGTCTTGCT ATGCTGCCCA GGCTGGAGGG CAGTGACTAT TAACAGGTGC AATCATAGCA 60
CAGTGCAGCC TCGAACTTGT TTTTCTGCTT CTTTTATACC TCCAGAGCAC CTGATATAGG 120
ACTGGCTCTG TACATGCTGG GCATTCCCAG GCCAGGGTAA CCAGACAGAC CCATGATACA 180
ACCTGCCAGC GAATCCCGGA AACTCCAGGA CAGGAGACAC TTGCAGGCTA ATGGTGGTGT 240
GCACCACCAG AGTCTTCGGC AGCTCACGGC CCTTCTATCT GCCTTAAGTT GCTGGGGCAG 300
AGAGCAGTGC CAAGGCAGAG AGGAAGGAGA ACATCCCTCC GTGTAGACCC CAGCTCTTCC 360
CTCCCCCTCT CCTCTGGGGC TTCAGCGGGT CCGGAGCTCA TGAATAAAGC TAATATTGGA 420
ACTAGTCGTA TACTAGTTGG AGAGGGGCTG TTGTCTAGAT CCTCCCTTGC AGGGACGGGT 480
TGTGCCAATA GAATGCCCCG AGGCCCCAGC CCTCTCGTGA TGGTTGGCTG GAACTAAGGC 540
ACCCCCCTCT CTCGCCCTTT TATGAGTCTC AGCTGATTTC CCTGGAGGGC GGCCCCACTA 600
GCCAGCGCCC CCAACCCGCT ACCGGACTCC CTCACTATAC CTGGGCCCCG CCCCAACTGT 660
CCTCAGGGGC GGGGCCAGCC CTAGGGCAAG CTGGGGCAGG AAGTGGTTGC AATTACACAC 720
ACTCCCGCCC CGCACTGGCT GCCACTGCCA GAGTGACAAT GCTAACTCGG CCGGCCCCAA 780
ACGTCAGGGC AAGGGCTAAG AAGAGGACTC AACCAGAGAA GCTCCTGGGC TGGAACGAAG 840
CTCTTTTCCT GAGAGAAGGG AGTTTCCGAG GTTAGGCTTG GTTGGAAGCC TCAGCGGATT 900
GTTGGTCACA TCCAGAGATG AAGGGAGGGG GTCGTGGGTC TCCTTCCCCA CCCAGACATG 960
GCAGTCACTC ACACCGTCAT CTCTTTTTAA CCTGGCCACT AGCTGACAGC AGCTTTTCCT 1020
AGCTGCTTGG GCCCCCTGCT CGCAACTGCC AAGACAGACA GCTCTGATCC CTCCTACCAG 1080
GGGAAGATGG GCTTTGATTC TCTACTACTG CAAACAACCA CAGCACAGTG GTTTCTATAT 1140
CCCCTACTCC TCCTTCGTTT CTTAGGCATT CCCATCTGGG GCGGCTCTGG GCCAGGTGGA 1200
GAGCGTGACT GGTATGGCCA CAGCTATGGG CTGAGAACCA TGTAGAGAGA GGGATGGATG 1260
GGGGAATTCG AGAATGTTTG GGTGGGATGA CTTCAGAACT CTCTGGGTTG GGCTTTCACT 1320
GAAAGCATCA TTAGCTCAAA AAATTGGGGC TACATTAGAG GAATGGAGGT AGAAGGGGGC 1380
AGTGAAGAAA CTGGACAAAT GAAAGAAGAT ACTTTAGGCT GGGCATGGTG GCTCACGCCT 1440
GTAATCCCAG CACTTTGGGA GGCCGAGCCA GGTGGATCAC CTGAGGTCAG GAGTTCAAGA 1500
CCAGCCTGGC 1510
|
