| Tag | Content |
|---|
EnhancerAtlas ID | HS180-10321 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr11:129672930-129674260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr11:129673644-129673659 | GCATGACTCAGCAGA | + | 7.23 | | Nfe2l2 | MA0150.2 | chr11:129673642-129673657 | CTGCATGACTCAGCA | + | 7.41 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27353 | chr11:129672992-129674302 | Esophagus | | SE_27846 | chr11:129672711-129673904 | Fetal_Intestine | | SE_28695 | chr11:129672475-129674371 | Fetal_Intestine_Large | | SE_35121 | chr11:129673024-129673979 | HeLa |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr11 | 129674047 | 129674142 | | chr11 | 129673400 | 129673800 | | chr11 | 129673800 | 129673805 | | chr11 | 129673676 | 129673819 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I129802 | chr11 | 129672728 | 129674240 |
|
Enhancer Sequence | AGCATGCAGA GGCTTGCATT GTGAATTTTA GCCCAGATTG ACTGCAAGAA AAAAACAGCA 60
ATCCTTAGAA GACCCAAAGA CCCTCTGAAG GAAGCAGACT GCTCCTGTGG GAGCCAGGAG 120
ACACCCTAAA TACTGTGAGT GCCCCAACTG CATAAGTGAG AAGGGAGATT CTCCTTTCCC 180
AAACACACAC CCCCACTAGA GAAGATGAAG GTCTGTTTGC AAGAGAAGTT TCCAACTTTA 240
CCTGGAGCTG AGTCAAGTTA GAGAGCTGAG CGAAATACAG GGGTACAGGA AGCACCAGAA 300
AGGCGCTGGG AGCTCACTAG GTCCCCAAGC AGCCCATTCC TGCCTGACAC CACAGGAATC 360
CATCGGGAGG GTGGCCAGAG GAGCAGGCGG TTAAACTCCA CAAGGAGAAG GAAATCTCTA 420
GCTGAACTTT GTAACAATTT GAAAGGGGTG AGAAGCCTCC TAGCCAGAAC TTGTGGGAGG 480
GCATGAATCT GGTGCACAGA CTTCACAGGC AAGGGGAAGA ACTAAAGCCA TTTTCTTTCA 540
CAGCTGGGAG GCACAAAGCC TCCAGTAAGT TTTCAAGTCC ATCCCGCCCT CTGCCTGGAA 600
ACAGACTCAG GGCTGTTGTG GGAGGCACAG TAGGAATGAG AGTGGCCCTT CGGTTTATAT 660
GGGAGCTGGG TGAGACCTGT GACTGCTGGC TTTCCCCCAC TTCCCTGACA ACCTGCATGA 720
CTCAGCAGAG GCAGCCATAA TCCTCCTAGG TACACAGCTC CAATGACCTG GGAATCTCAC 780
TCCCATCCCC CACAGCAGCC ACAGCAAGAC CCGCCCAAGG AGAGTCTCAG CTCATCACAC 840
CAAGCCTCGC CTCCACCTGA TAGTCCTTCC CAATCCACCC TAGTAGCAGA AGACAAAGAG 900
AATTTAATCT TGGGACTTCT AGGGTCCCAC CCACCACCAG TCCCTCTCCA CACTACTACA 960
GCTGATGCTT TCTGGAAAAT GCCACCTCCT GGCAGGAGGC CAACCAGCAC AAAAATAGAG 1020
CATTAAACCA TCAAAACTAA GGACCCTAAC GGAGTCCATT GCATCCTCCA CCACCTCCAC 1080
TGCAACAGGC GCTGGTATCT GCAGCTGAGA GACCTATAGA CAGTTCACAT CACAGGACTG 1140
TGTGCAGACA ACACCCAGTA CCAGCTTGGA ACTGGGCAGA CTCGCTGGGT GGCTAGACTC 1200
AGAAGAGAAA CAACAATTAC TGCAGTTTGG CTCACAGGAA GTCACATCCA CAGGAAAAGG 1260
GGGTGAGCAC TACATCAAGA GAACACCCCA TGGGACAAAA AAATCTGAAC AACAGCCTTC 1320
AGCCCTAGAC 1330
|
