| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00673 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:17612990-17614430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:17613334-17613349 | TGGGGTCAGGGGTCA | + | 6.67 |
|
| | 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 |
| GH01I017286 | chr1 | 17613436 | 17614463 |
|
Enhancer Sequence | CAGCTGATGA GTGAACTTCA TTCAATCTGC AACCTTCATT CCCTTTTACT AAGAAGGTCA 60
TATACTCACG AGTTCTGCAG ACTCGAACGT GGAAATCTTT GGAGGACCAT TTTTCTGCTG 120
ACTACAAGCA ACCAGGCCCT GACTGCCGTT TCTGGCCTCC AAGAGTGAGA CCATACCCGG 180
TCCCCTCTGA AATCCACAGA GGCAGCAGCA GAAAGATGCA GTCAATGAAC CCTCACTCTG 240
GGACTGGTGT TCAGTTCTGG ACCCTCCGCT GGGCTGAGAT CTGGGATCCC ATGGATGCAG 300
GCTGGGTGGC TCCAAAAAGC ACTGGAAGCT GCCTCCATCA GGCCTGGGGT CAGGGGTCAC 360
CTCCGCTGGC CACTGCCTTC CCAGACAGCT GCCCATGCCA CACTGCCTGG TCCCTTCCGG 420
GGCCTGGCTC TCAGGCCTGG AAAGCCCAGG GAGACTAGGA TGAGGCTTGG GTTCTCGTAG 480
GGAAATTTCC CTTCACCCTA TTGTGGTTCC CCTAACACAG TGGGCAACCT TGACCAGGCC 540
TGAGGATAAG GGAAGATACC CAACCGACTC ACCTACTCCC AGCTGGCTGC CTGAAACCCC 600
TCGGAGTTGG ACCATCAGAT GCTGAACTCG TACTCTCTAG CTGAGCACAT AACTTGGGTG 660
AGCCTCAGTT TCCCCCTCCA TAAAATGGGC AAAATAACTG CCGCTTCATA GAGCTTGCAT 720
GGGGATGAAG TAGGGTAACT CACAAGATAT ACTTAGTGTC AATAGCACAG TGCATGGTGC 780
ATAGTAAGTG CTCAGTAAAT GATGACTGCT GTTACATAAC ATCCCCCAGC CCTTCCTCAA 840
GCATCTGCTG TGTAGAACAC TCCTAATCTC CGCGCTTTAA TAGATGACAA AGACCCTTTG 900
AGACCCAGAG GTGAAATGAG GGAGGTAGGG ACAGGACAGC TGTCTTGGCT ACTCTCAGAT 960
CATACCCTGC TTGTCTCAGC TGTGTAGGAC TGGCCCAGGT GGAGGCTCCT GCCTGGACAA 1020
GAAGCTGACA AGAAAGCCTG TCTTTTTTGT GGGGATTTGC AGCTCTGGGT GGCCCTGACT 1080
CATGCTTTAT TCAGAATTTG GAATAAGTAG CTGCAGGGCT TCCGCAGGCA TTGCCCAACT 1140
CTGTGGCCTC CTGCGGCTTC CAGCAGCCCA GGAAGGAGGG CCCTGGGTGA GGATGGCTGG 1200
AAAGGAATTC TGGATGGCTG GACAGAGTCC ATGGGACCTA TCACTTCCTA CAAAGTCACT 1260
GTCATCCCAA GTCCCCTCCA GCATAATGAC GGCAAGTGCA AGCATTGTGC CAGCAGGTAC 1320
TGAATGCTTC CTGAGCACCA TCTGATATAG CCCTCACAGC ATGCCAGCAG GCAGCTATTA 1380
CTATTGTTCT CACTTTATAG ACAGGGAAAC TGAGGCACAG CCACATGAAA GCGCTTGCCC 1440
|
