| Tag | Content |
|---|
EnhancerAtlas ID | HS048-08015 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr11:129672730-129674250 |
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 | ACCAGTTAAG GATATAACAA ACAAACAAAA AAGAAAGAAA AGAAAACTAT AGACCAATAT 60
CTCTGATGAA CATAGATGCA AAAATCCTCA ACAAAATAGT AGCTAACCGA ATCCAACAGC 120
ATTATCAAAA AGATAATACA GGGGGATTTT GGGATCATGG CAGATGGGGG GCAGGACTAG 180
ATTGCAGCTC CAAACAAGGC AGCATGCAGA GGCTTGCATT GTGAATTTTA GCCCAGATTG 240
ACTGCAAGAA AAAAACAGCA ATCCTTAGAA GACCCAAAGA CCCTCTGAAG GAAGCAGACT 300
GCTCCTGTGG GAGCCAGGAG ACACCCTAAA TACTGTGAGT GCCCCAACTG CATAAGTGAG 360
AAGGGAGATT CTCCTTTCCC AAACACACAC CCCCACTAGA GAAGATGAAG GTCTGTTTGC 420
AAGAGAAGTT TCCAACTTTA CCTGGAGCTG AGTCAAGTTA GAGAGCTGAG CGAAATACAG 480
GGGTACAGGA AGCACCAGAA AGGCGCTGGG AGCTCACTAG GTCCCCAAGC AGCCCATTCC 540
TGCCTGACAC CACAGGAATC CATCGGGAGG GTGGCCAGAG GAGCAGGCGG TTAAACTCCA 600
CAAGGAGAAG GAAATCTCTA GCTGAACTTT GTAACAATTT GAAAGGGGTG AGAAGCCTCC 660
TAGCCAGAAC TTGTGGGAGG GCATGAATCT GGTGCACAGA CTTCACAGGC AAGGGGAAGA 720
ACTAAAGCCA TTTTCTTTCA CAGCTGGGAG GCACAAAGCC TCCAGTAAGT TTTCAAGTCC 780
ATCCCGCCCT CTGCCTGGAA ACAGACTCAG GGCTGTTGTG GGAGGCACAG TAGGAATGAG 840
AGTGGCCCTT CGGTTTATAT GGGAGCTGGG TGAGACCTGT GACTGCTGGC TTTCCCCCAC 900
TTCCCTGACA ACCTGCATGA CTCAGCAGAG GCAGCCATAA TCCTCCTAGG TACACAGCTC 960
CAATGACCTG GGAATCTCAC TCCCATCCCC CACAGCAGCC ACAGCAAGAC CCGCCCAAGG 1020
AGAGTCTCAG CTCATCACAC CAAGCCTCGC CTCCACCTGA TAGTCCTTCC CAATCCACCC 1080
TAGTAGCAGA AGACAAAGAG AATTTAATCT TGGGACTTCT AGGGTCCCAC CCACCACCAG 1140
TCCCTCTCCA CACTACTACA GCTGATGCTT TCTGGAAAAT GCCACCTCCT GGCAGGAGGC 1200
CAACCAGCAC AAAAATAGAG CATTAAACCA TCAAAACTAA GGACCCTAAC GGAGTCCATT 1260
GCATCCTCCA CCACCTCCAC TGCAACAGGC GCTGGTATCT GCAGCTGAGA GACCTATAGA 1320
CAGTTCACAT CACAGGACTG TGTGCAGACA ACACCCAGTA CCAGCTTGGA ACTGGGCAGA 1380
CTCGCTGGGT GGCTAGACTC AGAAGAGAAA CAACAATTAC TGCAGTTTGG CTCACAGGAA 1440
GTCACATCCA CAGGAAAAGG GGGTGAGCAC TACATCAAGA GAACACCCCA TGGGACAAAA 1500
AAATCTGAAC AACAGCCTTC 1520
|
