| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00864 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:27173410-27175090 |
Target genes | | Number: 27 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:27174587-27174602 | GAGGTCAGGAGTTCA | + | 6.22 | | ZNF263 | MA0528.1 | chr1:27175068-27175089 | TTCCCCATCTTTCTCTCCTCC | - | 6.25 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_23384 | chr1:27173604-27174629 | Colon_Crypt_1 | | SE_23384 | chr1:27174699-27178454 | Colon_Crypt_1 | | SE_24351 | chr1:27174710-27177316 | Colon_Crypt_2 | | SE_26621 | chr1:27173970-27186608 | Esophagus | | SE_34526 | chr1:27174651-27176664 | HCT-116 | | SE_50491 | chr1:27174691-27177388 | Sigmoid_Colon | | SE_53016 | chr1:27174654-27177272 | Small_Intestine | | SE_57686 | chr1:27174839-27175963 | VACO_503 | | SE_64263 | chr1:27174693-27178982 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I026847 | chr1 | 27174110 | 27178056 |
|
Enhancer Sequence | GAGTCTCCCA CCGTCGCCCA GGCTGGAGTG CAGTGGCATG ATCTCGGCTC ACTGCAAGCT 60
CCGCCTCCCG GGTTCAAGCG ATTCTCCTGC CTCAGCCTCC CGAGTAGCTG GGACTACAGG 120
CACACGCCAC CACAACCGGT TAATTTTTTG TATTTTTAGT AGAGACGGGG TTTCACCGTG 180
TTGGTCAGGA TGGTCTCGAT CTCCTGACCT CATGATCCGC CCGCCTCGGC CCCCCAAAGT 240
GCTGGGGTTA CAGATGTGAG CCACCACACC TGGCCAATTG TTCCCTAATT TTTGTTTGTT 300
TTTAGAGACA GGGTCTTGCT CTGTCACCCT GGCTAGAGTG CAATGGAGTG ATCCTGGCTC 360
ATGCTCACTG CAGCCTGGAA CTCCTGGGCT CAAATGATCC TCCCACCTCA GCCTCCTTAG 420
TAGCTGGGAC TATAGTCACA CGCCGTCATA CCCGGCTAAT TTTTGTCATT TTTTATAGAG 480
ATAGGGTCTT CCTATTTGCC CAGGCTCATC TTGAACTCCT GGGCTCAAGC AGTCCTCCCA 540
TCTTGGCCTC CCAAGGTGCT GGGACTACAG GCATGAGCCA CTGCATTCGG CCTGTTTCGT 600
AGTTTTTAAT CTGTAGTCAG ATTTCCACAG TTGCCCTCCA AATGTCTTTT GTTGCTGTGT 660
TTTGTTTTGT TTTTCAAAAT AAGATCCATG ATGTATTGCA TTTGTTTATG TCTCTTAAAT 720
CGCTTTTAAT TTAGAATCAT CTCCTCTCTG CCTCTCTTTC TCTCTCTCTC TTTTTTTTTT 780
AAGACAGGTT CTGGCTTTGT TGCCCAGGCT GGAGTGCAGT GGCGTGATCT TGACTCACTG 840
CAGCCTTCAC CCCCTGGGCT CAAGTGATCC TCACTCCTCA GCCTCCCAAA GTGCTGGGAT 900
TACAGGTGTG AGCTACTGCA CCCGACCTCC TCTCTCTTTT TATAAATGAC ATTGACTTTT 960
GTTAGAGATC AGGCCAGCAG TCTTGTAAAT GTCTCATATT CTAGATCTGA CTTTTTCCTC 1020
ATTGTGTTAC TCACTTTGTT CCTCCATCTC CTGAACCTCC TGTAAACTGG GACATAGGTC 1080
TAGGCTTGAT GAGATGCAAA TAAACCTCAC TGGCTGGGCG CGGTGCATCA CTCCTATAAT 1140
CCTGGCTGTT TGGGAAGCCA AGGTGGGCAG ATCACCTGAG GTCAGGAGTT CAGACCAGCC 1200
TGGCCAACGT GGTGAAACTC TGTCTCTACT AAAAATACAA AAATTAGCTG GGCGTGGTGG 1260
CACACTCCTG TAATCCCAGC TACTCGGGAG GCTGAGGCAT GAGAATCGCT TGAACCTGCG 1320
AGGTGGAGGT TGCAGTGAGC TGAGATTCAC GCCACTGTAC TCCAGCCTGG GCGACAGAGT 1380
GAGACTCTGC CTCAGGAAAA AAAAAAAAAC CCTCACTAAG CTTTCTGGGA GTCTCCTTCT 1440
CTGACAGCCC TTCTTAGAGT GGGTAAGGCC GGCAGGTGTA TGAACAGAGG CAGTCTCAGT 1500
ACATGGTGGC AGTTCCTAAT ATTTGTCCCT GCCTTAGGCC AGACATTTTA CTCCAATGTT 1560
TGTTCCTGGG AACCTGTTAC CCTGAGGCTT CTCCTGGACT GGCCAGGCAG CAGTAGCTTT 1620
CCCCTGCTGG GGATCCGGGC CCTGGGCTGC CTTGGGCATT CCCCATCTTT CTCTCCTCCT 1680
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