| Tag | Content |
|---|
EnhancerAtlas ID | HS040-20539 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr2:112374720-112377110 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr2:112376955-112376965 | TTCAAGTGGT | - | 6.02 |
|
| | 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 |
| GH02I111616 | chr2 | 112374341 | 112377462 |
|
Enhancer Sequence | GTCCTGTCTG TTCCCAAGTG TCTAACATCT AAGAGGGTTG GGTTCATAGT CTGGCTGAGG 60
ATATCCTTTC CCTCCCCTCC CATTTTTACT GTAAAAACAT TTTGACTAGA AAAAGAAAAC 120
CTCTTATATA CTCACTATCC CAGGCAAGAT TCTTCTTTTT TCTTTTTCCT CTCTGGTTGT 180
TTTTTTTGTT TTGTTTTTTT GTTTTTTTTT TTCATTTCCT TACATTCTCT GTGCATTTGC 240
CTATGCACCG TGGGATTTAA ACAATAGATT GGGAAAACAG TGGAGAGGGC ACTGAGGGTG 300
CCCTTTTGTG GTAGAAATTG ATTTTGCAGC CCTCCCCTCC CCCCCATACA CACGCACATA 360
CACACACTGG GTATTTTGTT AGTCTTAACC AAAGATCAAA ACAACATAGC CTTGACCTTA 420
ACTCACAAAC AGCCTCCAGC TACAGGGAAA AAGTCTCTGA GCAGGGGGAG TACAAGTCCC 480
ACCAGAGCCC TTATTGATGG CAATTTAACA ACAGGTATTT TATTTAAGGC CTGCATTTTT 540
CATACAGAGA CACAGTGACT CGGCTTTCAG GTATGTCTCA TAAGGAAGTA GGAATGGAGA 600
AAAGACTTGG GATTTTGAAT ATTTTACACA GCTTTACTGA TGAACAGTAA ACTGGAAGTG 660
ATCGCCATGT CTGACTGTAA AGGAATAGTT AAATAAATGT GCCACCCATG AGTAGAATGC 720
ATACCTTACG CACGTGTGCA TGCACCTTCT CCAGGCAGGA AGAGTTTCCT GTGCACCCCT 780
CACCTCCACC CATAGGAAGA GCTATGGGAC CTACAGGAAC TCCAGTGCTC CTGGGGCACT 840
CCCAGCCTGT GGCACTGGAG TGTCACGTGG ACAACAGAGG GTGGCTTTGT GGTCAGAACA 900
GCATGGGCTC AAATCCAGCT TGGTCTTGCC TTGGCCTGCG TAGCCCGGGC AGCTCTTCTG 960
CCTCCCCCAA CCCAGGGAAG TGGGGTTGAT GTTCTGAATC TGCAGGGCTC TTGGAGAAGT 1020
TACAGGGTGC CTGACACATG GGAGCCAGGC TCTGCCCACA GTCACCCAGC CAGCATGTTG 1080
CAGAGCCAGG ATTTTAAATT AGATCCAGCC AGTTCCAGAA TCATTACTTT TTCCGTTCCG 1140
TATGCATACC AGGCTGCCTC TTTCTAGATT ATCCTCCAAA AAGCCCTGGG GAGGCGGCAG 1200
CAGCATGAGC GGCAGACAGG CGGCCAAGAA GTGAGGCCCC AGACAGGGAT CTGAGCGTGA 1260
TCTTTGCCCT TGGGACGCAA GGCATCCATC CAAGAGGTCA CAGAAATCAG CAGCTTTCAC 1320
CGGGAAGCCC CAAGTCCTGG GATTGGGGTG CTGAAGGGGG ATCCAAAAAA AACAGTCATT 1380
GATTTGGAAG GAGATGCTGT TCTCCATCTC AGCCAGCTGT TAAAGGGACA TGGATTGAAC 1440
TCCCAGGCAG GGAGGGGCAT TTTGTTTCCC TTGGCCACAT CAGCATGTTT TTACAGTTGA 1500
GAGAGCAGGA GATGACTCTC CAGCCTGTGG CAGAGAGAAA GTGCCCTTGG CCCAACTCCG 1560
TGGAAGATGT TCCCCACCCC CCTTCCAGGA GAAGCTCCTG CTGGTGGATG CACGAACCCA 1620
GCTGGTGGCG ACACAAGGCC AGTGGGCACT CTCTGCCTTG CTGAGGCCTC AGCCTCCTGG 1680
CTGCGAAGGC CCCGGGTTCC CCTCTGCAGC CAAGTCTTTA CTTCCCCTTC ACCCTGAAAA 1740
ACGTCTTCAC AGACTATCAT TCTTGGTCTC TTGACTGCCT TTCTCCGGTT TCCTTTCACA 1800
ATCCCTCAGA GATGGGACAT CTCTCCAGAG GACGCCTGGG TTGTGAGGAT CTATGGTCAG 1860
AACATTTTGG TCAATGACAG ATTACATACA CCACAGTGGC TCCCTCAGAT TATAAAGGAG 1920
CTGAATAATT CCTATCACCA AGTGACAGTG CTATGCCATC TAAGCTTGTG TAAGTACACC 1980
CTGTGATGTT CACACAATGA CGAAATCACC ATTGTTAAGT AAATGGGTTT GGGAGAAGGT 2040
TCAAACAGCT TCCACCTGCC CCACCCTTCC GTTTCCTAAG CTCAGCCATG CCTTTGGAGG 2100
GTAGCACCTT TGTTTCTTCC ACATGTCGCA AATACAGTGA CACATGACTG TATTCAGGAA 2160
CAAGGAGGCT CTGGTGCAAA AAGAACATCA TTTCCATATG TGAGTGGGTC TTCTGGGTCC 2220
ATCACAGGCA GCCAATTCAA GTGGTCCATC CGTCAACAGA ATTCTTCTTC CAGGCTCACC 2280
AGGACTTCTT CCAGCCATAG CACATAACAT CATAGCACAA CACATTACCC ACGTGTTTGT 2340
GGCAGTGCTG ACGTCAACAC ACCTCCTGCA CTGCCAGGCC TGTAAAAGTC 2390
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