| Tag | Content |
|---|
EnhancerAtlas ID | HS129-00437 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:17613220-17614560 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
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 | | NR2F1 | MA0017.2 | chr1:17614474-17614487 | CACGTGACCTCTG | - | 6.04 |
|
| | 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 | CCTCACTCTG GGACTGGTGT TCAGTTCTGG ACCCTCCGCT GGGCTGAGAT CTGGGATCCC 60
ATGGATGCAG GCTGGGTGGC TCCAAAAAGC ACTGGAAGCT GCCTCCATCA GGCCTGGGGT 120
CAGGGGTCAC CTCCGCTGGC CACTGCCTTC CCAGACAGCT GCCCATGCCA CACTGCCTGG 180
TCCCTTCCGG GGCCTGGCTC TCAGGCCTGG AAAGCCCAGG GAGACTAGGA TGAGGCTTGG 240
GTTCTCGTAG GGAAATTTCC CTTCACCCTA TTGTGGTTCC CCTAACACAG TGGGCAACCT 300
TGACCAGGCC TGAGGATAAG GGAAGATACC CAACCGACTC ACCTACTCCC AGCTGGCTGC 360
CTGAAACCCC TCGGAGTTGG ACCATCAGAT GCTGAACTCG TACTCTCTAG CTGAGCACAT 420
AACTTGGGTG AGCCTCAGTT TCCCCCTCCA TAAAATGGGC AAAATAACTG CCGCTTCATA 480
GAGCTTGCAT GGGGATGAAG TAGGGTAACT CACAAGATAT ACTTAGTGTC AATAGCACAG 540
TGCATGGTGC ATAGTAAGTG CTCAGTAAAT GATGACTGCT GTTACATAAC ATCCCCCAGC 600
CCTTCCTCAA GCATCTGCTG TGTAGAACAC TCCTAATCTC CGCGCTTTAA TAGATGACAA 660
AGACCCTTTG AGACCCAGAG GTGAAATGAG GGAGGTAGGG ACAGGACAGC TGTCTTGGCT 720
ACTCTCAGAT CATACCCTGC TTGTCTCAGC TGTGTAGGAC TGGCCCAGGT GGAGGCTCCT 780
GCCTGGACAA GAAGCTGACA AGAAAGCCTG TCTTTTTTGT GGGGATTTGC AGCTCTGGGT 840
GGCCCTGACT CATGCTTTAT TCAGAATTTG GAATAAGTAG CTGCAGGGCT TCCGCAGGCA 900
TTGCCCAACT CTGTGGCCTC CTGCGGCTTC CAGCAGCCCA GGAAGGAGGG CCCTGGGTGA 960
GGATGGCTGG AAAGGAATTC TGGATGGCTG GACAGAGTCC ATGGGACCTA TCACTTCCTA 1020
CAAAGTCACT GTCATCCCAA GTCCCCTCCA GCATAATGAC GGCAAGTGCA AGCATTGTGC 1080
CAGCAGGTAC TGAATGCTTC CTGAGCACCA TCTGATATAG CCCTCACAGC ATGCCAGCAG 1140
GCAGCTATTA CTATTGTTCT CACTTTATAG ACAGGGAAAC TGAGGCACAG CCACATGAAA 1200
GCGCTTGCCC TGGTCACAGA GCTATTAAGT GGGGGAAACA AATTTGAGCC TAGACACGTG 1260
ACCTCTGTAC CCAGTCACAC CAGTGGTTCT CAACCCATCT ACACATTAGA ATCACCTGGA 1320
AGGCTCTCAT GAAAACCTAG 1340
|
