| Tag | Content |
|---|
EnhancerAtlas ID | HS170-00509 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr10:119563100-119564660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr10:119564387-119564404 | TGGAACACCATGTACCC | + | 6.9 | | Ar | MA0007.3 | chr10:119564387-119564404 | TGGAACACCATGTACCC | - | 7.72 | | NR3C1 | MA0113.3 | chr10:119564387-119564404 | TGGAACACCATGTACCC | + | 7.09 | | NR3C1 | MA0113.3 | chr10:119564387-119564404 | TGGAACACCATGTACCC | - | 7.81 | | NR3C2 | MA0727.1 | chr10:119564387-119564404 | TGGAACACCATGTACCC | - | 7.12 | | NR3C2 | MA0727.1 | chr10:119564387-119564404 | TGGAACACCATGTACCC | + | 7.26 | | ZNF740 | MA0753.2 | chr10:119563474-119563487 | CCTCCCCCCCCAT | + | 6 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I117804 | chr10 | 119564061 | 119564210 |
|
Enhancer Sequence | AGAAGGCTTT TGGAAGGCCA GGGTCCTTCA GGTGGAAGAA GAGCCTGTGC TCTTTGTAAA 60
CAGAGAACCC TATTCCCTCT GGTTAGGTAT TTTCCTCCCC CCCTCCTGGG AGACCTGCAC 120
TGTGCTTTGA GGAAACCTGT CAGTACAGGA CTCAGCCTTT TGGTGGACAA AACCAGAATG 180
GATCCCTAGG TCTGGTCTCT AAAGACCTTT TGAAGTAAGT GGGACAAAAA TGTCACCAAA 240
GTGCCCATTG CTTCCTTCTA ATGTCTTTGA AATGCTTCTC AAATCTCCTT CTTTGGCCTT 300
TAAGGCAGAC AGCCCTGCCA GTCACTCAGT CTGCCTATGC CTCAGTTGCC TTCTCTTACA 360
ACAAATCCAC TAATCCTCCC CCCCCATTGT ATGTTGTGGG AGCGAGGATC CCACGCAATC 420
ATACATGTGA ATGTAATCAT AATCCCACCA GCGAGTGTTT ATTGAGAAGC AGCTGATGCA 480
GAGACAGGGA CCCTCTCGAC AGCCCTACAG TCGAGTTCTC TTATCCTCCT GCTCTTCCAG 540
ATGAGGAAAC CAAAGTTAGA GATTAGTCCC TCGACAAGTC ACACAGCTCA TATCGGTGAC 600
TTTGCAGAGC CTGCCCCCTT AGGCTCTGTG CTATCCTAGG TTGTATTTCC AGCTGTTATT 660
CTAGTGCTGT GAGTTTTTGC TCATGCGTGG TGTGTCCGGG AAATTGATTG CTCCAGTCAC 720
TGGGGGCATT CTAAGAAGAG TTCCTAAACC CCACCCCTCC CCCGATCCCC AGGCCTCCTA 780
GGTTCCATTT TACAGATGGG AAGGACATCA CTGAGGGCAG GGGTGCAGAG AGAAGAGGGT 840
AAACGAATTA CTCCAGCCCC AGAAGGAGTG CTGGCAGCTT GGAATAGTTG CAGCGCAGAC 900
CGGGTTTCCA CTCGGCTGCC TCAGCCACAC TCCTAGAGCC CGGCTGATAA TTGCTCATTA 960
TGTGCTTAAT CTGGGCACAG CCGGGCCTGG CAGCAGAATT GCATCACATC AAAGAGAGCT 1020
CTTCAAAGCA GCAGAAAGCT GGCCCCTGGG GTAATTAGCA GAGGGCCTAT TCTTTGCTGC 1080
TTGGGACAGT TGGAAGGTTT CGGGCAAGGT CCAAATTGCA TGAAGCGAAG CTCTGAGTCG 1140
TCAATTCTCT GGTGAACTCA GACAGGCAAG GCTGATGACT CAAATCATGC CGTTTATTTA 1200
TTTCTTCTTT TATAAACTGC TGAGACATTT TTTTTTTTCT GCCAGCCTGG CCCAGATGCC 1260
CTGATCAACT GATTGTCCTC TGCCTCCTGG AACACCATGT ACCCTCTCTC TAGGCCGCCG 1320
TGTTCTAGGA GGAACCGAAA GAAAATATAT TCACGCACAT ACACACATCA CCACCATGAC 1380
TCAAGAAGAA AACCTGGAAG AAGATGACAG AACCTTGCTT GTGCATAGAG GTGCTCTGAA 1440
TCACATCACC ATGACTCAGT TTCCCCAGTT ACCTGAGCTG AGGGGCCCCA GGTGGCAGTC 1500
CTAGCTTGGG GAGTGTTGGT TCATCCATCA AAGTGGAACT TAAGGGGCAA CAGGCCAGGT 1560
|
