| Tag | Content |
|---|
EnhancerAtlas ID | HS051-23197 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr6:27654980-27656380 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox3 | MA0514.1 | chr6:27656244-27656254 | AAAACAAAGG | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 27655000 | 27655243 | | chr6 | 27655152 | 27655475 | | chr6 | 27655751 | 27655869 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I027687 | chr6 | 27654780 | 27656741 |
|
Enhancer Sequence | TAACAGAAAC AGTCGTGGTA GGAAGAGGGG GAAAGTAGAA ACTTGTCAAA AAACAGACAG 60
TAAATCATGA ATTAGCTGCT CCAGTGGCCC CTTCCTGGGT TGTCACCTGC CAGCAAGAGC 120
ATCAGGCTCC GTCTGGAAGC GGGGCACCTC TCAGGGGCAA ATGTTTCACG CCTGCTTCCT 180
CTGAGTTGTC GAATCCGGGC CTCGCCTCCT CCTCCCTTTT CAGATCATAG GATTTCTCTC 240
CCCCGCAAAT AATGGCCCTT ACTTCGTAAA CACGCTGGCT CCGTAATCCC TATTATTGTT 300
TTGGGGGTTT GGTTCTGTCC AGGGAGGAGG TGAGGGCAGA TGCTCAAGAG AGGCTGTCCC 360
CACCGTCCTT TTGTCTCAGC GAACCGCAGT CCGCGCCCGA GCGCCACTAG CTGTCCTGGG 420
ACGGGAACTG CAGCGGCAAG TGTGTGACTT TCTTGAGCCC GGAGCCACAG GCCTGGGAAG 480
CGCCGCTGAG ACTTCAGGGT CGTAGTGACA GAGGAACCAC CCGAGGCTAG GCGGGGAGAG 540
GGTGCAGTTT CCGGATCCCG AAGGCTTCGA GAAGAGCCGA CCTGTCTGGA AGGGTCTCCA 600
AGAACAGAGA GGACTCTGCA ACCATCACTC GGGAGCCGCG TCCTTTCATC CTTGAGACAG 660
CTCCGTGGTC CAACGGTTCC CCGATCCGCT GGCCGAGATC TCAAGCTTGG ATGCAACTTC 720
GGATTCGCCC CAGGCAGGAG GAAGGAAGCC CCGATTGGAA ACGTTGACTT GAATCTTCTC 780
GGATCAGAAT TAGCAGGTTA AGAAAAACTG TTTCCCCGTA AGAAGCAGGG TTCTTTGGTG 840
TTCAATGTGG AGCTCCGCCA CTCCCAGCCC GGGTGAAGGA AAACTGGGAA ACAGAATGAA 900
TGTGATTATC TATTCGAAGA TAAATTTCCA CAAAGCATGC CGTTTGATAG TAGCTTATAA 960
TGTGGAAGTA AGGCATCCTG TCATCCGGCC GGTTAGCTCA GTTGGTTAGA GCGTGGTGCT 1020
AATAACGCCA AGGTCGCGGG TTCGATCCCC GTACTGGCCA AGTATTCTCT GTGGCTTTTA 1080
TCACCAGAAT GGATAGTAAC CCAGACATCG ATCTAAACGT GTACCTGTGT GTTTCTCCAG 1140
GCTTAACTTT GCCCCGAGAA AACGGATCTG TGAATTTGGT GCGCCCTCGC TTACTCGACA 1200
GCGGTTAATT TGAACGGGGA CGTTTCTTTC CGCTGCCTCC AAGGCATACC CACATCCTAC 1260
CCGTAAAACA AAGGGGCTAT AGGCACCTTA CAGTGACAGA GGTACGTTAC GGTTGGAGGC 1320
TTTTGTGATT TTTGTCCTCC TCTGCCCCGG GGAAATTTTC TTGGAGTAAA ATACTGAATT 1380
ATTTGATTAC TTCCAAAAAA 1400
|
