| Tag | Content |
|---|
EnhancerAtlas ID | HS101-42119 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr8:22600620-22601580 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr8:22601519-22601534 | AGGCCAGTGTGACCT | - | 7.12 | | STAT3 | MA0144.2 | chr8:22600783-22600794 | CTTCCCAGAAG | - | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_24334 | chr8:22600513-22601243 | Colon_Crypt_2 | | SE_24334 | chr8:22601318-22601594 | Colon_Crypt_2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I022741 | chr8 | 22599459 | 22607261 |
|
Enhancer Sequence | CCAGCCTCCT GTCCCCAAGA AGCCCCAGGC CCTTATCAGT GCTTCCTTGG GCTACCTGAC 60
CTCCCCTTGG GCTGCCCAGC TGCTGGGGCT GGGGAGTGAG CAAGGGCAGT GAGAGTGAGG 120
CCTGCCTGAG AGTGGAGGCT ACTGACCTCC TGGGCAGGAC CTCCTTCCCA GAAGCAGAAG 180
CAGAGCTCCC TTTGGGGGAG AAACCCCCTC AGTTTCTACT GTAATAAAGA AGGGGCCTGA 240
GCTCTTGCTG GAGCCTCTAA TGACGGGGTT GAGGTGTAAT GAATATCTGT GTACTCATAA 300
AACAGGCTAA TGACGGCCCT CGGCCCTCAT TTTATGGACC CGTTTCATCC TTACTTGTTC 360
CCAAACCAGA AGGGACCATC CTGGGGGCTG AGCCAGGAGC CTGATGGCAG CCCCAGACCA 420
CAGCTGTTTG GAGTGGGGGC TAAATGGTTC CTGAGCCTGA AGCCCCTCCG GAGCTGCCTT 480
TTCCTCCTCC ATCCCTTATC TGGTTGAGAC AAAGTGAGGA ATTTAGGTCA ATGGCTGACA 540
ACAACCAGCC TTAGGAAATG GGCAGGGGAC AGGGAGGGAG GAAGTGCATC CACCCTGATT 600
CTTAAGAGTG TCAACACTTG TCACACATGG AGGCCAGAAA GAGCATTCAG CACCTGCCGG 660
CAGCACCACG CCCCTTTCCT CTGCCCAGGT ACTGATAGGA GCTCCCTGAA TCATCCCAGT 720
TGCAATTCCA ACACCTGAGC AGAACTAGAC TCCGTGGAGG GTGGGGCTGG CCCGCTGAAT 780
CACCAGTAAC ACCTGTGTTT TGCTTGTGAG GTCTCCCTGC TCACTCGGGG ACCAGCCAAG 840
CCTGACCCTG TTTGGCTTCT CGGAGCTTGG TGAGATCACA GCCTGGGGGT TGTGGCTGCA 900
GGCCAGTGTG ACCTGCTGTG CAGGGAGTAT TTTTAAAGAG ATACTTGCCC TGTGTTCCCA 960
|
