| Tag | Content |
|---|
EnhancerAtlas ID | HS040-24478 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr22:42671040-42672860 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr22:42671746-42671757 | GGCTGTGATTT | - | 6.02 | | TP53 | MA0106.3 | chr22:42672128-42672146 | CACATGCTGAGGCATGCT | + | 6.01 | | ZEB1 | MA0103.3 | chr22:42671443-42671454 | CCCACCTGCCC | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_25072 | chr22:42671093-42671976 | Colon_Crypt_3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH22I042275 | chr22 | 42671094 | 42671976 | | GH22I042276 | chr22 | 42671992 | 42672730 |
|
Enhancer Sequence | GTTTGGAAGA GGCTGAGCTG GTATTTGAAC CCAGGTTTTC AGAGGCTGCA CTCTTAACCA 60
CCAAGCTTCC CAGCACTCAG CAAACACTGG AAAGACAGAG ATGGACCTAG ACAGTCAGTA 120
GGACCAAAAG TCTGCAGGCC GATAGGGAAA GAATGTAAGA GGACGGCATG GGCAGCGCCA 180
GCCCCTCCAG CAGTCATATA TTAAGCCCTG GACACTGGGC AGCTCGGGCA GGTCGGGGGG 240
CCTCAGACTC TCGGACCCCA TGCCTGGAAG ACCACGGTCT GCCCAACAAG CAGCAGCTGC 300
TGTGAATCGA CTTACACATC TTCCCCACAG GTGAGCAGAG AGCTAACACC TGAGGATAGG 360
CCAAGAAACG GGAAGCCCGT GCAACCTGAG CGCACAGATC ACCCCCACCT GCCCGGCACT 420
CACTGTCCCC AGTGGCTGGA CTCTCATCGG GCCAGTCACT GAGCTGGCGC CAGCCTGGTC 480
TCACCAGTGT GTGTCTTTAA ATCATCCAAT TTCTTCAGCT GTAAATTGGG CTGGGAGGGG 540
CCAGGTGAGC TGCCTGCCTC AGGGGAGTCG GCGCCCTTAC CTGAGTGATC CCATTCACTC 600
CTCACAACAA ACCCATGAGG CAGGGATTGT CATCTTCATT GTACAGAGCA GGAAATGGGT 660
GCACACAGAG GTTAAGAGAC TTGCCCAGGT CACACAGCTA GGAAGAGGCT GTGATTTGAA 720
CTCAGTCTTC TGGCTCCAAA GCCCCCACAG AGTCACTCAG GGCACTACAA AGAGTTAACC 780
TGAATATGAA ATGATCTAAG AGTCGCAGTG ACAAAGGCAT GCTCTAAGCG CTTTTCCTGC 840
AGTAACTTGC TTAATCCTTA CAACAACCCT ATAAAGTGGG TACTGTTCTC GCCTCATTTT 900
GCAGATGAGG AAACTGAGGC ACAGAGCAGC TCGGAGGGGG CAGAGCTGAA TCTGACAGGC 960
TACAGGGCCC CTGCGTTGCT TTGTTATAAG ATGACAATAA GGAAGTTCCT TTCCTTTGGG 1020
ATTATTTCTG CCTGAAAGCT CAAGACTTTT AGCCACATCA TTGTCTGGGC TCCACGGGAA 1080
GGCAGTGCCA CATGCTGAGG CATGCTGGGA AAAGACTTTG TTCCATCCTG TTTTGTTGAC 1140
ATGCTCTTCA TTTTTAAGCC TGAAACCGAA GCTTCCTGCT AAGAATTCAA ACCATGGAGA 1200
AAAACGCAGC CATGATAACG GCCACTACTT CCTGAGCCTC CAGTGTTCCC TGTGCTTGGG 1260
GATCCATATA TGTCACTTAA CCTTAACCTT CACAACACCA GGGCAGCCTC CATTTTCACA 1320
AGTGAAGAAA TGGAGGCCCA GAGTCACTTA GAAGATGCTC GAAGGTGCAC AGCTGCTAAG 1380
TGGTGGTGCT GGGATTTGTC CTCAGGTCCT CAAGAGTCCT GACTCTTATG TGCTGGCTCC 1440
CCACGGAGGC GTGGAGTCTT GTTTGCTGGG CATTTGACAG AAATGTTTCT GCTCATCTTC 1500
TGCCACAGGT TGGTCCTTCA GCGTCAAGAT TCCTGGGCCA CTTATTAATA GAAGGCACCA 1560
GGACACAGGT GCAGGGATGC AGAGCTGGAT GCTGCCTTCT CAATAGGAGA AGCCAAGAAA 1620
CGCAGATGCC GATGCTTAAT CAACTCCGTC TCTCCCTCTA GTGACTCGGG GATAGCTGCC 1680
CTGATGCCAA GGCGATTGTC TTCTGGAAGC AGCCACGCCG TGTGAGGTTC CTCATCACTG 1740
CCCTGCATCT CCCTGCGAGC TCTCGGGGAT AATTGCAAAA TCACGTTTGA TTCCAGGGGA 1800
GCAGAAAGCA GCAGGAGCCG 1820
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