Tag | Content |
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EnhancerAtlas ID | HS129-32697 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr6:159268780-159269650 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MNX1 | MA0707.1 | chr6:159268943-159268953 | GGTAATTAAA | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr6:159269524-159269539 | TGAACTCCTGACCTC | - | 6.22 | PHOX2A | MA0713.1 | chr6:159268945-159268956 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr6:159268945-159268956 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr6:159268945-159268956 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr6:159268945-159268956 | TAATTAAATTA | - | 6.62 | RORA(var.2) | MA0072.1 | chr6:159268954-159268968 | TAAAATTAGGTCAT | + | 6.06 |
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| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_23109 | chr6:159269528-159270215 | Colon_Crypt_1 | SE_27140 | chr6:159268671-159269476 | Esophagus | SE_27140 | chr6:159269496-159270180 | Esophagus | SE_27853 | chr6:159268889-159276361 | Fetal_Intestine | SE_28795 | chr6:159268853-159276331 | Fetal_Intestine_Large | SE_34137 | chr6:159268799-159269423 | HCC1954 | SE_34137 | chr6:159269472-159272352 | HCC1954 | SE_34769 | chr6:159269432-159276667 | HeLa | SE_35994 | chr6:159268630-159276489 | HMEC | SE_52705 | chr6:159268945-159269415 | Small_Intestine | SE_52705 | chr6:159269488-159270224 | Small_Intestine | SE_58403 | chr6:159210147-159292283 | Ly1 | SE_64395 | chr6:159268761-159270224 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I158847 | chr6 | 159268541 | 159279766 |
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Enhancer Sequence | CATCTCATTT TCTTGAAAAG GCCCAAGTAA AGTAGATAGA TTTTCCAAAC TGTTAGAGGT 60 TGAATTGTGT TTCCCACCGA AAAAAAAAAA AATCCTCTGT TGAAATCCTA ACTTCCCCAG 120 TACCTAGGAA TGTGACTGTA TGTGGAAATA GAGTCTTTAA ACAGGTAATT AAATTAAAAT 180 TAGGTCATTA GTTGTGCTGT AATCCAATAT GGCTCATGTG TTTACAAGAG GAAATCTGGA 240 CAGACAGGTG CAGGCATGTG AAGACACAGG CAGAAGACGG TCATCTGCAA GCCGAGGTGA 300 GAGACCTCAA AAGAAACCAA CCTTGCCGAC ACTTTAATCT CAGACTTCTA TTTGACAGGA 360 TGATGAGAAC ATAGATTTCT GTTGTTTCAG CCACCCAGTC TGTGGAATTG TGTTATGGCA 420 GCCTGAGTAA ACTAACACAC AATCCAACCT GGCTAGCACT CCTACTCTCA AAGCCCAGGT 480 TTCACTCAAT AATTCCAAAC CATGGTTCAC TTCTTTTTTT AAAATTAGTA TTATTATTTT 540 TTGAGATGGA GTCTCACTCT GTCGCCCAGG CTGGAGTGCA GGGGAGCAAT CTCAGCTCAC 600 TGCAACCTCT GCCGCCCAGG TCCAAGCAAT TCTCCTGCCT CAGCCTCCCG AGTAGTTGGG 660 ATTACAGGCG CCAGCCACCA CGCCCAGCTA ATTTTTGTAG TTTTTAGTAG AGATGGGATT 720 TCACCATCTT GGCTAGGCTG GTCTTGAACT CCTGACCTCG TGATCTGCCC GCCTTGGCCT 780 CCCAAAGTGC TGTGATTACA GGTGTGAGCC ACCGCGCTCG GCCATTTCAC TTCTTATTAA 840 TCACGACCAG TGTTTCCTGA GCACTTACCA 870
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