| Tag | Content |
|---|
EnhancerAtlas ID | HS051-25083 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr7:72981940-72982990 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx3-2 | MA0122.3 | chr7:72982958-72982971 | ATTAAGTGTTTTT | - | 6.42 |
|
| | 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 |
| GH07I073568 | chr7 | 72982401 | 72982550 |
|
Enhancer Sequence | CAATTACTGC CTTCACATGC AGGATTTTTG ATTAAAAAAA AGAAAAACCT TGGTGGCCTC 60
TGCTCTATGT TAATATCCAG ACACCTTCTC TGTGGTTACA AGAGAAGCTT GAGTGAGGGC 120
ACTTTCTGTC CTCAGAAGTC TGTGGAATGA CTTTTTGGTA GTGTTTTCTC GTCTCACTGA 180
AACACAACAT GGCAAGGTGG GTAGCACAGG ATTCATTCTT ATTTTGCAGC TGAGGAAACA 240
AGCTCAGAGA GGTCAACGGA CCTACTATCT GCTCTCCAGC TGGAACTGGA ACTGAAGACA 300
TCTGACTTCA GTAACTCAAC ATTCTACTGC CACTTCCTGT CCTGGATACA CAACGGGAGT 360
AATGCCAGAG CTGCTTCTAA GAACAGGTGC GCAAAGGAAG TGTTTTAGTC TCATTCTTCT 420
GACAATTGCC AAGGAAATAC TCCTCAGGCC TTGTGTGCAC AGCATTGCCA AAAGTCTGTG 480
GTTAGGAACA TACAAAACCA CAATGGAGAC TGGGAGTGGG AAGATGCGCG GAGAAGATAC 540
TGGGAGGTCT GTGGCTTGCC CCTGGCTTGA GTTTCACATT GAGTGCTTAC ACTGTCCCAG 600
GTACTGTGCC TGGACCACAG AGCTGACAGT GGGATGGTCC AGGAGTCTGC CCGGTGGTGC 660
TCTCATTCCA GTGGGTTCAA CAGTGAGCCA GAAGCTGCCA ATAAGAGAGT AGTGGACTGC 720
ATCGGGCCGA CCTTAGTGTT TTGTTTGGTC CAGATAGTGT TTAGTTATTT AAGTTGCTCA 780
CTTCTAGCTT CTGTGAAGCA ATTTCTGCTG GATTCCTGAA TAAGTAGCAG CCACCCCCCA 840
TCCTGCAGGC AGGACACAAG CCCGCCCTCC AGCTCACTTC TGTCCCCACC TTCTACTGCC 900
TTACACCCAG GTAACTGACC CTTCACACAT TTACGGTGCC CATCTGACAT TCATAGCATT 960
TAGAGGGGGG ACGAAGCCAG GTTACACAGG ACCTTGCAGG CCATGGTAAG AATTTTGGAT 1020
TAAGTGTTTT TAGCTAGGCA CGATGGCTCA 1050
|
