| Tag | Content |
|---|
EnhancerAtlas ID | HS052-07699 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr11:119107320-119108100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr11:119107660-119107673 | GAAAATTCTAGAA | - | 6.71 | | NFAT5 | MA0606.1 | chr11:119107656-119107666 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr11:119107656-119107666 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr11:119107656-119107666 | AATGGAAAAT | - | 6.02 | | NFE2L1 | MA0089.2 | chr11:119107347-119107362 | ATTGCTGAGTCATAT | - | 7.68 | | Nfe2l2 | MA0150.2 | chr11:119107349-119107364 | TGCTGAGTCATATGG | - | 6.37 |
|
| | 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 |
| GH11I119237 | chr11 | 119107761 | 119107910 |
|
Enhancer Sequence | ATATATATAT ATACCCATAG GAGTGGAATT GCTGAGTCAT ATGGTAATTC TGTGTTCAAC 60
TTTTGAGTAA CCTCCAAACT ATTTCCACAG TAGCTGTACC ATTTTTCTTT CCCCTAGCAA 120
TGTATGTGGG TTCTGATTTT TTGCTAACAA TTGCTATTGA CTTTTTTTAT TACAGCTATT 180
CTACTAGGGG TAAAGTGGTG TCTTGAGGTT TTGAAATGCA TGTGAATACT TTTTCATGTG 240
CCTCTTGGAT GTTTGTATAT AGTTGTCCCC CTTTATCCTC AGTTTAACCT TCCTTGGATT 300
CAGTTACTGG CAGTCAACCA TGGTTTGAAA ATATTAAATG GAAAATTCTA GAAATAATTC 360
ATAAATTTTG AATTGCATGC CCTTCAGAGT AGTGTGATGT AATTTCACAA CGTTCTACTT 420
TATCCCAGCT GGGATGCAAA GCATCCCTTT GTACAGCATC TCCATGCTGT ATACACTAGC 480
ACCTATTAGT CACCTAGTAG CTATCTTAGT TATCAGAGTG AGAAAACATA ATATACACAG 540
GGTTCAGTAC TATCTGTGGT TTCAGGCATC TGCACATCTT GGAATGCAAA GGGGGACTAT 600
TTATCTTCTT TGGAGAAACA TCTATTCAAA TCCTTTGCCC ATTTTAAAGT TGCATTATTT 660
GTCTTTTCAT TGTTGAGTTG TAAGATTTTC CTTCATATTC TGGATGCTAG ACCAGATACA 720
TGATTTGCAA AACTTTACTC CCATTCTGTG GGTCATCTTT TCACTTTCTT AACAGTATGC 780
|
