| Tag | Content |
|---|
EnhancerAtlas ID | HS146-02507 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr11:10396510-10397300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr11:10396654-10396669 | TGACCTTTGACCCTG | - | 6.22 | | NR2C2 | MA0504.1 | chr11:10396654-10396669 | TGACCTTTGACCCTG | - | 7.66 | | Nr2f6 | MA0677.1 | chr11:10396654-10396668 | TGACCTTTGACCCT | - | 7.82 | | Rxra | MA0512.2 | chr11:10396654-10396668 | TGACCTTTGACCCT | - | 7.95 | | ZNF263 | MA0528.1 | chr11:10396845-10396866 | TCTCTTTCCCTCCCCTTCTCC | - | 6.44 |
|
| | 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 |
| GH11I010374 | chr11 | 10395984 | 10398272 |
|
Enhancer Sequence | CTTAGAGGTA TAAAACTGGA GTGGCAACTG ATTCCCAGAA CTTTAGAGCT CTCTCCTCTT 60
TTTCAAGGTT CTGGGATGGT ATGTAAGTGT ATCCCTTCTG CCTAGCCAGC TTTCCTATCT 120
CTAGACCGGA GAGGACCCTC TCTCTGACCT TTGACCCTGC CATACCTAGC ACAGGACTTA 180
AAAGTGGCTC CTGTTGCATC CCATGGCGAG TGCAGACAGC CCTATCCTAT ACCCTTTTCA 240
TTCCTCTTAG CTTGGTATAC AACAGTCTTT TCCCCTAGTT TATAATCTGT GAGGGCTGAC 300
ACTATGTCTT GTTCATCCTG GGAGCTTGCA TAGCTTCTCT TTCCCTCCCC TTCTCCACGT 360
GCCTTGCATA CAATAGAGGA TCCCAGCAAC ATTTGTTAAA AAACCCATCC CCGGATGCTC 420
CTCTAGACAG TACTATCTTC TCCTTTTTGC CCTATAAACC AACTGCTGTG GCTTTAAAAC 480
TTTGCATTGT TGGCCAAGGG TTCTGAAACT GCAGTTTGTC TTAATCTGTG GTCTCTGGAT 540
TCTTGCTTGA TTGCTCTCTT TCTGGAAATC TCCCAGATAG ATCACAGCCA GTCATATCCG 600
CACTGCACCT CTCCCCAGGA TAGTCAGCAT GAGGGCAGAG GTAGAAGGGC CTTGAGAGAG 660
CATCCAGGAA GCCCTTGTAT TACAGATGGG AAAGCAAAAC CCCTGAGAAG AGAAGGGATT 720
TGCCTGAGGT TATGGTTTTG AGTCAGGGCC AGAAATCAGC TTTTCTGTCT CCCAGAGCCC 780
CCAGGGCTCC 790
|
