| Tag | Content |
|---|
EnhancerAtlas ID | HS101-38454 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr6:127804860-127806200 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr6:127805436-127805457 | AGTATGAAACTGAAACTACAC | - | 6.5 | | IRF8 | MA0652.1 | chr6:127805439-127805453 | ATGAAACTGAAACT | + | 6.74 | | IRF9 | MA0653.1 | chr6:127805438-127805453 | TATGAAACTGAAACT | + | 6.24 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_33154 | chr6:127803203-127806518 | H1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I127481 | chr6 | 127802459 | 127806459 |
|
Enhancer Sequence | TGTTTCAAGG ACAAGCGTAA TATGATCTCT GGTGCTCAGT TCCATTTCTC ACACCAATAT 60
AAGAAGAAGG GTCTCTGTAT GTAAACAATA ATTATCCGTA TGTATGACTG TCTACCATAT 120
ACTACACATT GAGGGGGAGA CTCAAAGTTT GATTAGATAC TGCATCTACC ATCAGGAAGC 180
TGAAACTTAG CAGGGGAGGA GACAGAGAAG CAAACAATTA CAGTGCAAAT TGATAAATGC 240
TATGCTTTAG GTTCTGTGAA GCAGGGGTTT TGATTTAGTG TGGCATCACC ACCATAAAAA 300
TAGTGCTTGC CACATGGCAG GTGGTGAAAA AAATACTTGC TGAACTAATG ATATATGAAT 360
ACCAAATCGA GGTTCTGAGG TCAAAGAGAA GGACAGGGGT ATAGACTGAC AGTAAAAATA 420
GGGAAGCCTT TTCCAAACAG GAGTCTTCAT AAATTCGCAA AGAAATGAAA ATTAAATTCT 480
TCACATGTTA ATTTCTAACC CATATCCACT GTTAAGTAAA GGCATACGTT CAAGCACAGA 540
AGGCAGGGGA ATACTTTGGT GCAACTGCTT TCATTCAGTA TGAAACTGAA ACTACACAGA 600
CAAATGAATA GCCCACGTGG TTATTCATTT CTAGTTCTTT ACAGGAAGAA GTTCTTTCTG 660
TTGCTTGTAT AATCTTCTTA GAAAGGAAAG CTTGGGGACT GACTCACCAT AACCAAAAAG 720
TAATTTAGGA AGTAATCAAC AAAACAGTCC CAAGAATACC AAGAATAAAG TGAGCTAAAC 780
TAAGAAACCT GGAACATTCT AGGTAGGGGC TGCCTACAAG AAGCGTTGAA TTTGTTTCAC 840
TAAATACTTA TTGAATGCTT GTATTTGAAT TCACTCAATT ATGTGTTTAT TTAGTGACTA 900
CCAATGCACT TCATAACATA CCTGTGACAC AATAATAATG AAACCAATGT GATCTTTGCT 960
CTTTTGGGGG TTCTCAGCTT ACTTGGCATG ATCTGTTCAG TCTGGAATTC AACACAGTGT 1020
TATGAAAGCA ATGATAATAC AAGAACAATA TTAACTGTCA TTGAGCCCTA ATTCATGTCA 1080
ACCCCTTCAC ATACATTATC TCAGCTAATT TTTAAACACT CCTTTTAGCC TCACTTTGCA 1140
GGTGCTGAAA CTAAAGTTTA CAGGGGTAAC AGAAGTAGAT GAATAAATTA TCAAAAGCAT 1200
CAGTTATCTC TGTGCTCCTC AGAACAGCAT CATCAGTGTC ACCCAGAAAG CTGTTGGAAA 1260
AGCAAATTCT TGAGATTCAT CCCAGAACCA CTGATTCAGA AACTCTGAGG ATGAGGCCCA 1320
GTGATCTATG ATTTAATAAG 1340
|
