| Tag | Content |
|---|
EnhancerAtlas ID | HS040-06133 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr11:13359800-13361600 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr11:13359903-13359916 | ATTACATCATCTT | - | 6.82 | | JUND(var.2) | MA0492.1 | chr11:13359902-13359917 | GATTACATCATCTTC | - | 6.41 | | NFE2L1 | MA0089.2 | chr11:13360170-13360185 | TTTGCTGAGTCACTG | - | 6.81 | | Nfe2l2 | MA0150.2 | chr11:13360172-13360187 | TGCTGAGTCACTGAA | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_19448 | chr11:13359051-13362690 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_36817 | chr11:13353194-13361966 | HMEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 13359856 | 13360227 | | chr11 | 13360424 | 13361428 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I013337 | chr11 | 13359091 | 13361942 |
|
Enhancer Sequence | TTTCATTAAG AGGAATTTGT AGAGTTATTT CTGGGGTCAG GCAGGATACA TTCAGACGAA 60
CATTTTAGAT CTAGGGCTGG GAAGATCCCG AGACTCGTTA TAGATTACAT CATCTTCCTC 120
CAAGTGCACT TGCCAGGCAA ATGGACAAGT GCATTTTAGA AAGGTTTTCA GTTGTTCACG 180
TTTAAACAGA AAGGATCACC TGGCTAACTT TTAGTTAACC CATTGAACAG ATGTGCCATT 240
CCCCCAGCCC ATTGGTTATT CATGTCCTTG TTACTGGTTT TTGATATCCT TGCCCCGTAG 300
GTGGGAGGAG GGATGGGTAT GAGCCTGCCC TGCCCTCTTT CTCCTACTTG GGACAGAGCT 360
GTTGCTTTTA TTTGCTGAGT CACTGAAGCA ATAGAGCATG TGCAGAGTCC CAGCCTGGAG 420
GTGGGCATAT CTGGGTTCCA GTCCCTGCTC TAGCCCTTCT CAGCTGTGTG ATCTTGGACA 480
AGTTGCCATA CCTCTCTGAG CCTCAGTGTC ATCTTCTATG TGATGTCGAT GCCTCCCCCA 540
AAAGGTCGTT ACGAGGACCA AAGGAGACAC GTCAGGGCAG GAACCATCCT AGGCACGTGT 600
TTGATGCTCA GTAAACGGGA CGTGGTCAGT GTTCAGAGTT GTGGGGGTGG CAGGTGACTG 660
CTCTGTTTCA CCTCCACTCA CAGCAACAGG GCCTGTGGTG TCACCTAGAC ATCTCATAGG 720
CATCCCACAC TGAACATGTC CCAAACCAGC AGCTCCTCCC TGGATGGGTG GATGGTGTAC 780
AGGGACCTCT TCCTCCAGCT GTCACATGGG GCATGTACCT GGCAAGTGGC TTTGCAGCCC 840
TAGCTGCCCC CTTGGCTGGG GGCCTTTGTG CAGTTCATGG ACTGGGAGTC ACCCCCATGT 900
CTAGACCGTC AGGAAACCCA TTGGCTTTTC CTTTAGAGCA TACCAAGAAT CAACTTCTCA 960
GAACATAGCA AGAGTTGACT TTTTGTCACC CTGCCGTGGC CACTCAGACT GACTCCTCTT 1020
ACACCTCACA TCCCATTGAT CAGCACAGCC CCTGGAAATA TGTCTAGAAT CCAGCTGCTT 1080
CTCATCACCC CCACACCTAA TACAGAGGGC TGAGTCATAG CATCTCTTCC CCGGACTGTT 1140
GTAGCCGTCT CCTAACTCAG CTTCCTGCCC TGCTTTTACA CACACACACA CACACACACA 1200
CACATGGTAT CTTCTCACCA CTGCAGCCAG ACTTAAAACC TAAGAGGGAT CATGTCACTC 1260
CCCATTTTAC TCAGAGTCAA GGCCAAGATC CTTACTGGGG TCTGCAGGCC CCCACACCTG 1320
GCCCTCTGAC TGCACCCCTA CCTTCCTTAG CTGTCTCCTC TCCCTAGCAT GCCCCAGGTC 1380
GCTGGTCCCC TAGCACTGGG CAGCTCCCTG CGGCCCTGTT CACTAGCTGT CCTCTGCCTG 1440
GAACACATCT GTCACCTCTC ACCTCCTCCT GTCCAGCCTC CTTGGGGCCT TTCTAACTGC 1500
CTCCCTCCTG TGGTCTGCCT CCTCCCCATC TCTGACTTTC CTCCCGAGCA CTTACTGCCA 1560
TCCAGCACCC GACATAACTT ACTTGTTTCG TTTGCTTGCC TTCCTCACCA GGAGGTGTGC 1620
CAGATGAGGA CAAGGATTTT TATATCCCTA CCCCCATCTG CAGCACTGCC ATGGAGAACA 1680
GTGCCTGGCA CTTGGATGCC CTCAGTAAAT ATTTGTTGAG AGACTAATAA GTGATCGTGG 1740
GCCAGCATGC CAACAGTGTC TTCGTTATTA CAAAATTGTC CCGAATTGAA ATTTGGCTAC 1800
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