Tag | Content |
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EnhancerAtlas ID | HS185-00045 |
Organism | Homo sapiens |
Tissue/cell | T98G |
Coordinate | chr1:8949960-8950860 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:8950345-8950366 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | IRF1 | MA0050.2 | chr1:8950628-8950649 | ACTTTCTTTCTTTTTTTTTTT | + | 6.09 |
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| Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
SE_10095 | chr1:8949953-8950644 | CD14 | SE_24627 | chr1:8950092-8950345 | Colon_Crypt_2 | SE_27088 | chr1:8949121-8950731 | Esophagus | SE_29363 | chr1:8949167-8950114 | Fetal_Intestine_Large | SE_30509 | chr1:8949331-8950649 | Fetal_Muscle | SE_34103 | chr1:8949014-8951315 | HCC1954 | SE_34433 | chr1:8949046-8951619 | HCT-116 | SE_34916 | chr1:8948890-8951553 | HeLa | SE_36553 | chr1:8948928-8950994 | HMEC | SE_42834 | chr1:8949081-8951314 | Lung | SE_46612 | chr1:8949058-8951353 | Osteoblasts | SE_47312 | chr1:8948889-8950974 | Panc1 | SE_53985 | chr1:8950030-8950630 | Spleen | SE_56056 | chr1:8948952-8950757 | u87 | SE_67633 | chr1:8948952-8950757 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I008889 | chr1 | 8949136 | 8951212 |
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Enhancer Sequence | TTTAGAATAT CTCTGAGATT ATTTGTGAAA CCTCAAGATT AAAAAAATAA CAACGACAAG 60 AAACAAGGCT AAGAATCAAC ATCCCAGGCT CCTGCCTCTT ATTCTATTAA CCACAGAAAT 120 TAAGTTCCGC AAAGACAAAG ATGCTTCTGT TACTTCCCAA TTAGTCTGCC CTGTTTGGAC 180 ACAGTCCCAG ACCTCATACC CCGGAGCCTA CGCACGGACT CCTGGCAAGA GAGGCGCCAT 240 CCCAGGCCCA GTGCCAGGGC TCCTCTCTCG GTCCTGTCCT CAGGGTGTCC TTGGGCTCCT 300 TCTGGACAGA GGCTCTTCCC TCTCCTGCCA GGTCCTCAGA TCCGAACTCC CTAAGCAGGG 360 GCTTATGTCT TGCCAGTGCT TCTTGTTTTT CTTTTTCTTT TTTTTTTTTT TGAGACGGAG 420 TCTCGCTCTC TCAAAAAAAA AAAAAAAAAA ATCAAATGGG AACACTTCAG CTATGACAGG 480 AAATATCTTC TCTATTTACA TAGGGCATAT GCCGAGTACA TGATTTTGTA ACTTTATTTC 540 ATCCTCTTCA TTTACCTAGG GTGTATACCA AGTAACCAAT GGAAACCTCT AGAGGGTATT 600 TAAACCCCAG AAAATTCTGT AACAGGGCTT TTGAGCCCTT ATGCTCAGCC TGCTCCCACC 660 CTGTGAGTAC TTTCTTTCTT TTTTTTTTTT TTGAGACTGA GTCTCGCTCT ATCGCCCAGG 720 CTGGAATGCA GTGGTGCGAT CTCAGCTCAC TGCAGTCTCC GCCTCCCAGG TTCATGCCAT 780 TCTCCTGCCT CAGCCTTCCG AGCAGCTGGG ATTATAGGTG CCCGCCACCA CGCCTGGCAA 840 ATTTTTTGTA TTTTTAGTAG AGATGGGGTT TCACCATGTT AGCCAGGATG GTCTCGATCT 900
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