| Tag | Content |
|---|
EnhancerAtlas ID | HS092-03032 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:118229070-118230520 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA | MA0071.1 | chr1:118229658-118229668 | TGACCTTGAT | - | 6.02 | | Znf423 | MA0116.1 | chr1:118230329-118230344 | ACAACCCAAGGGGGC | + | 6.11 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_43509 | chr1:118228261-118230163 | MM1S | | SE_67143 | chr1:118228261-118230163 | MM1S |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I117686 | chr1 | 118229601 | 118229750 |
|
Enhancer Sequence | GAAGAAATCC AGCAGGAGGC AACAGTGGGG TATGTGGAGT CCTTAGATAG GCCACTGTCT 60
AAGGCAGGCA GCTGGACCCC ATCCTGAGAA TGAAACTGTC ATGGGAGCTG CAGGTGGGTA 120
CAGCCGCCCC AGCCCTCCTA GGGGTGCTCT CTGCCCACTG CTGGTTGGCC CCACCAAGTG 180
CAGGCAGCAC AGTGAAACCA GACACAGCAC AGTCTCAAGT ATGCAACTGC CAGGTATGAC 240
AATCACAAGT CACAGCTGGC AGGTGGATTG GTGTGATGGC TGCTCATGTT TTCTGATCTC 300
TCAATTTTGT TCTTGTTTTC AAAAAGTAAC CCAGCAGGTT TAAGGTTCAC ACAACCTGTG 360
TAACTTTGAT TGCAAATACC AAGACCTCAC CTCAATAAGC AAAACAAGGA ATTTATTCGT 420
CTAAGAATCC TGACATGTAG AACAACCAAG CCTCAAGGAT GTGGCTAGAA CAAGAGACTC 480
AGATGCCACC TATTATTTTG TTCTGTTTAT CTCTGCCTGT CCCTTCATCA CTGCAATCCA 540
GCTTTCTGGA AACATGACTG GCCATAGCTT CCACTATGAG AGGGAGTCTG ACCTTGATTT 600
CCTCAAGGTC CGGTTAAAAA TTCCTGGGGA AGTTCATTGG TTCAGCATGA GTCAGAGACC 660
ATCCCTGGGT CAGTTAGCTG GGGGGGTGGG GACATGCAAG AATCAGGACA CTCTTGCCTT 720
GCTATGGGGC TGAGAGCAGG CGGGGTAGAC AGTTCTATGG ATGTCCACAG CTTATATCTA 780
ACCTGGACAT CAGATGTTTT ACAAGTGTTA GTAGCCACCT AAGGGCTGAT GTCACTGTCA 840
CTTCTTCAGC AGGGCACAAC CCACATCTTT AGATGGCTGG AAAAAGATCC TGGGCTAGGA 900
GGCTTCCTGG GGGAGAAGGG AGGTGTGGGG CTCCAGGTGC ACAGGGAGCC TCCCCTTCAG 960
GTGTCTTTTT ACTCCTGTCC CTCCCAGTGT CCCACTCACA CACCCCACTC TGTTGTGCCA 1020
GGTGTTCCTG TGGGTCGTCC TTGCAGAGTG AGCAGCAGAG CATTGGTGTG TGCTCGCATT 1080
TCAGACGCTT TGGCTGGCAG AGTTCTTTCC CTGCTATTCC ATTCCCATGC CACCCTTCCT 1140
CCTCTACCAG TATGTCCTTC CTTGTGGAAA AATAGCTCTT CTAGTAGTAG AAACTGATCC 1200
TGGGTCTAAG GGCAAAAGGG GCAGAAGGGA GGTTTATTGG AATGATTCTG GAGTATCTCA 1260
CAACCCAAGG GGGCTGTGGG AAGGTCAGAG CAGGGCCGCT GTAGGGCCTC TATGGTGGGA 1320
GTTCACGGAC TCTATGGTGC TGCTGATCAC ACGACTCAGC TTCCACTGAG TCCAGCCCCT 1380
TGCTGCTCAG AGCCATGCTT CACCTTCCTG GGGAGGGAGT CGAGGGGCCC CAGTTTGGTC 1440
AGTTATGTGC 1450
|
