| Tag | Content |
|---|
EnhancerAtlas ID | HS108-07041 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:14443560-14444840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:14444584-14444605 | CCCTCCAGCTCTCTCTCCTCT | - | 6.12 | | ZNF263 | MA0528.1 | chr11:14443920-14443941 | CCCCCCTCCTCCCCCACCCCA | - | 6.37 | | ZNF263 | MA0528.1 | chr11:14443914-14443935 | TCCTTTCCCCCCTCCTCCCCC | - | 8.18 | | ZNF263 | MA0528.1 | chr11:14443911-14443932 | TTTTCCTTTCCCCCCTCCTCC | - | 8.69 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 14443709 | 14444714 | | chr11 | 14443887 | 14444060 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I014421 | chr11 | 14442816 | 14446605 |
|
Enhancer Sequence | TTAGCTAGGC GTGGTGGTGC ATGCCTGTAA TCGCAGCTAC TGGGGAGGCT GAGGCAGGGA 60
GAATTGCTTG AACTCAGGAG GTGGAGGTTG CAGTGAGCCA AGACTGTGCC ATTGTACTTC 120
AGCCTGGGCA ACAGAGCGAG ACTCAGTCTC AAAAAAACAA AAACAAACAA AAGAAACCGA 180
GGCTCAAAGA GGTAAATTAA CATGTTCAAA GTCACGTGGC TATTAAGTGG TAGAGCTGGA 240
ACTTGAATAG GGTTTTTTTG ACTTTACATC TGGCACCTAA GCTCCTCTGC CACATTCTTG 300
AACTCAGTTC TCCAGCATAT CTCAGTGTAT CCAGAAGCAA TTTTTCTCCC TTTTTCCTTT 360
CCCCCCTCCT CCCCCACCCC ACAGGTCTCC ACCTCCCAAG TCCACAAATG CCAAACTCAC 420
AAGTCATCTG TTTTGCCAAA ATTCTGTTCC GATTTGATAA ACCCTAGCTG GGCCAGCTCA 480
CTCAGCATGA TTCAGCCGGA GAGAATAGCA AGGCTGCATG CCCGGCATGC CGACCAGCTG 540
AGCTCAGGCA GGATGGGAGG CGCTCAGGAA CCTCAGCCTG ACAGATGGCT CCACTCGGCT 600
GTCTCCACGG GCCTGATGCC AGGGGCAGCA CTCGTTCTCA GCAGGAGGGA GGTCGTACGA 660
GTTTCACATG CATGGATGTG TGTGTGTGTG TGTGTGTGTG TGTTTCACAT GGACCATGCA 720
GGAGTGAAGC TGTGTATTAT CCAGAGTGCC CATGTGTATG TGGCCGGTTT GCACATGTTT 780
GTCTGTATGC GTGTGGATGA ATGCATGTGT GCATGTCTAG CTGTGTGTTT GTGTGTGTAT 840
TTGTGTGCAT GCAGAAGTGT ATGTGTGTGT GTTTGAGTTT CAAATTTGCA TTCATGTAGG 900
ATGTGTGCTC ATGAGCATGA AAGAGAAAGC TGGGGGTGGG AAGTAGGGGG AGAACGGTCG 960
TGGGCTTTGA GAGTTGAGAA TGTTGAATGT TCCCACCTGC AGTGGAGAGT TGCTGTATGC 1020
CCCTCCCTCC AGCTCTCTCT CCTCTTCACA GGACTGACTG ACATCAGCAG CAGCAAAAGG 1080
TCATATCAAG CCCAATGTGA AGTTTAGGCT CTGGCTATGA TTTAGGTTTC CCAAACCAAC 1140
TCCTTGGCTA CAGTTTTCTC CTAAGGTAGG GGTACTTAAC TGTTTGTTAA TCTAGGGTCC 1200
CCCTGAAAAA TCTGGTGACC AGAATGAATC TTCCAGGAAA ATGCCCTCAA AACACATAAT 1260
TTTATATGCA ATATTATGGA 1280
|
