| Tag | Content |
|---|
EnhancerAtlas ID | HS118-03716 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr11:77169740-77170760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:77170130-77170151 | GGAATGAAACTGAAACTGTCT | - | 6.4 | | IRF8 | MA0652.1 | chr11:77170133-77170147 | ATGAAACTGAAACT | + | 6.74 | | IRF9 | MA0653.1 | chr11:77170132-77170147 | AATGAAACTGAAACT | + | 7.34 | | Nr2f6 | MA0677.1 | chr11:77170598-77170612 | TGACCTTTGACTCC | - | 6.47 | | Rxra | MA0512.2 | chr11:77170598-77170612 | TGACCTTTGACTCC | - | 6.53 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_28264 | chr11:77169721-77171458 | Fetal_Intestine | | SE_29510 | chr11:77169866-77171484 | Fetal_Intestine_Large | | SE_43997 | chr11:77166393-77169851 | MM1S | | SE_43997 | chr11:77169961-77170900 | MM1S |
|
| | 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 |
| GH11I077458 | chr11 | 77169991 | 77171357 |
|
Enhancer Sequence | GGCTAATTTT ATAAGTCCCT ATAGATAACA AATGAACTTC AATACTAATT ATAGTGCAAA 60
GGACGGAGAG AGTACTACGA AAATTCAAGA AAGTTTGATG AATATATGTC GAGGGAGTGC 120
AAAAGTAAAT TATTTTATTC AGTCTTTCAA CAAATATGTA TTAAGAGCCT ACTACATGCC 180
AGGCACTGAT CAAGATACTG AAGATACAGC AAAGAACAAA ACAAAGTACT ACCCTCTAGG 240
AACTTAAAAT CATAAATGGG AGGATGAAAA CTGGGGAAGC CTACATGGAA GAACTGGCAT 300
CCAAGTTGCA TCTTGAGGAA TAAAGAGTTT TAAAAGCATA GAGGAAAACA GAATTCCAGG 360
CTGAGGGAAC AGGGTAATAT GATATGAAAT GGAATGAAAC TGAAACTGTC TATTTAGAGA 420
GATAGAGTAG GGTTAGAAGA GATGATGCTG AAGAGGTAGG TGAGGTCAAA TTATTAAGTT 480
CCCTGAATAA CTAATTTACA TATTATCCTA TAAACAATGG AGACACACTG ATGGCTTTTG 540
GGAAGAACAG TGACAGGATC AGAAAAATTA CTCCAGGCAG AATAATGAAT AAATAAGAGG 600
GCACAAAGAC TGGTTGCCAC GACACTAGTT AATAGGTTAC TAAAAGTCAA GGGAAGAGAT 660
GATTACAGTC TAAATCAGAG CAGAAAGGAT AGAGAAATAA AAATAAACTG GTAAAAAAAA 720
CTACAGAGAT AAAACTAACA AGGCTTGATA ATCCATTGGA CTGATAGCAA GAGCTTATTC 780
ATTCTGCAAA TATTTACAAG CCTCACTGTG TTCCAAGCAT TGTACTAAGT GATGAGGTAC 840
AATGGTGACC AAAAGACATG ACCTTTGACT CCATGGAGTT GAAAGTCTAG ACATAACCAA 900
GAGTCAAATA AATACAGAAT CACAAATCAT TATAAATGCC ATCGCAGAAA ATAACAAAGT 960
GCTGTAAGAG GAAAACAGAG GGGCTCTTCT TCTTCTTTTT TTTTTTTTTT TTTTTGAGAC 1020
|
