| Tag | Content |
|---|
EnhancerAtlas ID | HS095-18141 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr20:6699200-6700230 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr20:6699868-6699879 | TCAAGGTCATA | + | 6.62 | | Esrrg | MA0643.1 | chr20:6699868-6699878 | TCAAGGTCAT | + | 6.02 | | RORA | MA0071.1 | chr20:6699867-6699877 | ATCAAGGTCA | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27865 | chr20:6698568-6700569 | Fetal_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I006718 | chr20 | 6699148 | 6699914 |
|
Enhancer Sequence | ATCCACCCTT CCACTAATGC ATGATGTTAA CCATGCCTCT CTTCCTTAAC TCTGTAGGCT 60
GGAATCTAAG CTGGGTAACA AAACGTAGAA ACTTTTCCAT GGTCTGACCC CTGCTTCATC 120
CTCCCATCTC ATCTCCTACC CTCGCCTCAC AGTTTGTGTT TAGATAATAT TGTGTCACAT 180
GAAGTTCTCC AAGTCCACCA CACTCAACCA TGCCTTCCTG GTTCTCCTCC GAAGAGTCTG 240
CCTGCTTGCC TTGTCCCCAT CCCCCTCTCC TCAGTACTGC TTACTCATTC CTGAAATGCC 300
AGCTCAGGCA TCAGGCATCA TTTCCCCCCA GGCAGCCTTC CGTGAACGTG CAGGCCGGGT 360
TAAGTGCCTC CTCTCTCCAC CTACAAGATA ATTTTATCAC GGCACGAATA GTATAGTGCT 420
GAAATCATCT TTATGATCCT GCTCCCAGAT CTGACTGAAA ACTTCTTGAG GGCAGGAGCT 480
GTGTCATATT CACCTCTAAA CCCCACAGAG ACAAGAGCCA TGCTAGACAT ATAGTAGGTT 540
TTCATAAGCA TTTATTGAAG TAAAGAAAAT AATTCAACAG GGTTGGCAAT TAACTAAATG 600
TGGAAGTAGC AAGACAGAGG GAGATTGGAA GCTGATTCCA AAGTTTGAAG TCCAAGTTAA 660
CTCAAAGATC AAGGTCATAT TTATAGAAAC AGGGAAGTCA GAAGGAGGAA CTTTTTTGAA 720
AGGAAAGGAA AAAAAAAACC CTAATGAGTT AATTTTTAAA CAAACTGAGT TGGAGATGCC 780
AACAAAATAT GCAGTTAGAA AATAGACCCT GTGGTACTAG AAAAAGGCCG TGGTAGGTTT 840
GAGGGTCATT GAATTTGTCA TAGTTTAGTA GATTATGCTG CCTAACAAAC AGCCCCCAAA 900
TCTCAGTGGG TTATAATTGC AAAAGCCTAT TGCTGCTCAC ACAGCATGTC TCCTGTGAGT 960
CAGTTGCAGC TCTGCCTGGG GCTTTGTTAA CTCTGTTCAG GTTTACGTGT GCATCTGGTG 1020
CGTACTGTTC 1030
|
