| Tag | Content |
|---|
EnhancerAtlas ID | HS007-16237 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr7:157069320-157070660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr7:157070589-157070604 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24015 | chr7:157069584-157070234 | Colon_Crypt_2 | | SE_25085 | chr7:157069574-157070296 | Colon_Crypt_3 | | SE_26907 | chr7:157069252-157070245 | Esophagus | | SE_68745 | chr7:157069590-157070363 | H9 |
|
| | 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 |
| GH07I157275 | chr7 | 157068250 | 157071071 |
|
Enhancer Sequence | GGCCAGGACT CCCAGCCACC CTTACCACCC TGTGCCCTGA CACCCAGCCA GCTCCTCACC 60
TAAGACCCAT CCAACATCTT GGACTATCAT TCAAGGAGGA AAGACACCTT GATCCATCTT 120
CAGAGTCCCA ACATTACTAA GACAGCCACC TAAGACACCA TGAAAGGAAG GCTGGTCACA 180
ACAAGGACTG ATGAGGCAGG AAGTGCCTGA TAAATTCACT CAGAATGTGG TCATTGCTTC 240
CTGGATACAA TGAAGTCAAC ACTGAAAACT CACAGGAGAG AAGTCCCCCT GGAGGGAGCC 300
TCCCCTGTCT ACTGGGGGGA CTGTTTCGCT GTAGCAGTGT GGGGCCATCC ACTCCCTGCT 360
TCAGGGCTAT CCCCCGTCTA CTGGGGGGAC CATTTGTCTA ACGGGGCAGC ATCACCCACT 420
GCAGGAATCA CCCCTGTCTA CTGGGGAGAC CGTCCCCCGT TCAGTCTGGG GCCTCAGCCT 480
CTGAGGCAAG CAGGGGAGAA CCGGGCAGAG TCTGTTGACT TCGGATGGTC CTAATGGCCT 540
CAGTTTCTGA GCAACTCCTT TCTGCGTCTC CCCACACCGG CGCTCCCGTT CCTCCAGCCA 600
GGCTCCCGTG TGTCCTCCTG GTGCCTGTCC TTCCCCCGGG TGTGGGCTCC TTCGCAGGCG 660
CTGCCCACCC CCCACCTCCT GCAGCCACTC ATGGCCGGCT CTGGGCCCTG GATCCCCGGA 720
AGGCACACAC ATTGAGGAAG AGGCTGTGTC TCCTCTCCCC TCCCCTTGCC GGGCTGCTGG 780
GGGCAGTCCT TGGCCGGCTG CCCATCTGTG CCATCGTCTG CACAGAATGG AAAGTGAGCG 840
TCTGTCATGC TCAGTAATTC CATGTCTGTT GAATCTAATA TCAAAAGATC TGGGCATCTG 900
TGCTGTGTGT CTGAGTTTTT TCATTTCATT TTCTAGTGAT GAGTGTTGAG TGCAGGTTGC 960
CACATACAGA GCAGCGAGAC CGCTGGACTT TCGCTCTGCC CAGTGCTTGG TGGCCCCCCA 1020
AGGAATGTGT TAAGTGACCT CCTTTATTTT TATTTTGTTT TATTTTTTGA CACAGGGTCT 1080
CCCTCTGTCG CCCAGTCTGG AGTGCAGTGG TGCGATCTGG GCTCACTGCA ACCTCCATCT 1140
CCTGGACTCA AGCGATGTTC CTGTCTCCGC CCCCCGAATA GCTGGGATGA CAGGTGCGTG 1200
TCACCGTGCC CAGCTAATTT TTGCATTTTT TGTAGAGACG GGGTTTCACC ATGTTGCCCA 1260
GGCTGGTCTT GAACTCCTGA CCTCAAGTGA TCTGCCCGCC TTGGCCTCCC AAAGTGTTGG 1320
GATGACAGGT GTGAGCCACC 1340
|
