Tag | Content |
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EnhancerAtlas ID | HS105-44281 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:85184740-85186020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr2:85185844-85185861 | GGGTACGTCCTGTACCT | - | 6.05 | EWSR1-FLI1 | MA0149.1 | chr2:85184888-85184906 | GCTTCCTTCCTTCCTCTA | - | 6.04 | EWSR1-FLI1 | MA0149.1 | chr2:85184880-85184898 | TCATCCCTGCTTCCTTCC | - | 6.06 | EWSR1-FLI1 | MA0149.1 | chr2:85184884-85184902 | CCCTGCTTCCTTCCTTCC | - | 8.57 | Foxd3 | MA0041.1 | chr2:85185139-85185151 | GAATGTTTTTTT | + | 6.52 | Zfx | MA0146.2 | chr2:85184773-85184787 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_24195 | chr2:85185151-85185630 | Colon_Crypt_2 | SE_25084 | chr2:85185063-85185733 | Colon_Crypt_3 | SE_27502 | chr2:85184750-85187659 | Esophagus | SE_32926 | chr2:85184713-85187023 | H1 | SE_34685 | chr2:85184438-85187655 | HeLa | SE_35873 | chr2:85183583-85187716 | HMEC | SE_47378 | chr2:85183405-85188185 | Panc1 | SE_52528 | chr2:85184768-85187231 | Small_Intestine | SE_64856 | chr2:85184623-85187455 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I084956 | chr2 | 85183648 | 85188352 |
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Enhancer Sequence | GGGATGGTCT CGATCTCCTG ACCTTGTGAT CCGCCCGCCT CGGCCTCCCA AAGTGTTGGG 60 ATTACAGGCA TGAGCCACCG CGCCCGGCTG GGAATGTGAT TTATTAATAA GATCAATGAA 120 TTAAAACATT GAAGTTGCTC TCATCCCTGC TTCCTTCCTT CCTCTAAGCA TCCAGAGAGC 180 CCTCTGATCC TTTGGGATCA CAGACATGGG ATATTTTTAC TCTCCAGCAT GAACACATAG 240 GTGGATTTAC TGTGAAACTA CTGAAGCTTA CACTTCAGGG TCCCTGGCTT CCTCAAACAG 300 GGCTTCCAAG CCCTATATCT AATTTTGCAC TTCTTTCTTA AGAGTTGCCT GTACCAAATA 360 TATAAGCCTC AGGGCCCCAA ACCTGGATCC AGCCTGAGTG AATGTTTTTT TAGAGCCAGG 420 TCTGATAGAA GCCTGTTTTT AAGGAATTAC CAGGAACTGA GCATGCTGTT TTTGGCCCTC 480 AGGGGTTTCT CTCAGAACTA AGAATTTGGG GGCTGTCCTC AGTCACAGGT GCAGCCTGAA 540 GTCTGTTCCC GCCATGTTCA CTCTCCTCTA TTTACCATCA CCTGCCCCTG CTGCGTCTTC 600 CTTTAAAATA CAGCCCTGGG CCCTAAGCTT TGTGCTGATT CAAGCTCTTT GGAATTCAAG 660 ACATCCAGGA ATCCGACGCT CCAAGAATTT TCCCAACGAC CTCTCAGTGG GCCATTCAGG 720 CAGGAAAGGA TACACACATT CCTAATGGGG CCAGGGGCTG TGACTTAGCC TGTGTGTGGC 780 TGAGAGCCTG CTGAATACAA GGTGCTGGCA GTTGGCAGGG CTTCCCAGGG TGGGGACTTC 840 TTGCTGAGCT CATCAGCAGG CCCAGCTCTG TACCCATTTG TCCAGGGAAA AACCAACCCC 900 TAATGGAACT GTTTGTTTTA TACTCTCTCA TCGAAGTCAT AAATGACTCA CAACTAGAAT 960 GTTATTAACG TGAGAACAGA GGCCTACCTG GCAGAATAAT TGGTTTTGGT CATTTGCTCA 1020 GAGTGCCAGG CAAATCCACA AAGCATATCA AATTACAGGT TAGAAACCTG ATGAATAAAC 1080 AAGAATAATA CTGTGAGTTC TCAAGGGTAC GTCCTGTACC TGTTTTGCCC ACTGTCATAT 1140 CTCCGGCAAG ACACAGTGAA TACAGCCCCT GACACATTGG AGGTAATCTA TAAAGAGTTA 1200 CTAAATGATT AAAGAAAAGG GATGAGCTGT TCTTAGTGGA AACACCCATT TCTCCTAAGA 1260 TGAATTCGCA TTCTTTTGGA 1280
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