Tag | Content |
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EnhancerAtlas ID | HS108-33053 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr5:149780000-149781190 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr5:149780926-149780944 | GGAAAATGAAAGCTGTAC | + | 6.73 | SREBF2 | MA0596.1 | chr5:149780673-149780683 | ATGGGGTGAT | + | 6.02 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_05618 | chr5:149780210-149781990 | Brain_Cingulate_Gyrus | SE_08000 | chr5:149779001-149782690 | Brain_Inferior_Temporal_Lobe | SE_09932 | chr5:149779647-149783339 | CD14 | SE_10161 | chr5:149777807-149781736 | CD19_Primary | SE_10893 | chr5:149777402-149801284 | CD20 | SE_13751 | chr5:149779737-149781989 | CD34_Primary_RO01536 | SE_14245 | chr5:149780353-149781613 | CD34_Primary_RO01549 | SE_53000 | chr5:149780449-149781665 | Small_Intestine | SE_53773 | chr5:149780942-149781823 | Spleen | SE_60838 | chr5:149777715-149800070 | DHL6 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I150398 | chr5 | 149778107 | 149782966 |
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Enhancer Sequence | AATTGGTGGG GAAGGCTTCC TGGATGAGGT GGCATCTAAA CTAAAGGATG GAACTAAAGG 60 ATGGTCATGG TTGATTTCCT GTTGCCAGAG TAAGTCATGT AAATACCCAA AGACAAGAAA 120 TGGAAGGGGC TGAGAATCCT CGAGTTAGGC CTCGAGCTAG GGGCAGGCTC CCTGGAGGTG 180 CCTGGTGAAC AGCTGTGGCA GGCACAGCAG GTCTAGGAAA ATCGGAAGTG AGTTGCCCCT 240 CAAATCGAGC TCACCATGGT TCTGTGGTGG TGAGGGCAAG AAGTGGATGA ACATGAAAGA 300 CAGGATGATG TCTTGGGTGT GGACTGAGGG AGGGGAGGGA TAGCAAAGGA GGTGGTCTGC 360 TGCTCCAGCC TGGAAATGCA GAAGCCCACT TCCCTGGGCC CAGAGCCATG TGGAACACCA 420 GGGGTCCTGG AGATGGTCTC CAGAGCTTTT AGCCTCATGC TGGAAACAGC CAGAGGCAGT 480 GCAGAAAAGG AATGCATGGC TGGAGGTGTC GGAGACCCAG GTTGGCATCC AGCTGCACCC 540 TTGACTCGGG GCCCGGGGCC AGACCCTCCA CCATCTGGCC TCTCTCCTCT CAAGCATGTT 600 GCTCTAGAAC AGAACTACAG AGTAGTGTCC TCATTGGGCC TTGTTGACCC ACAGCAAGAC 660 TTTAAACTTA AAAATGGGGT GATTTCACTG CAGTTCTTGA TTTCTGGCTC CTCTTAAAAA 720 GATAACATCT GGCAACGGGG GCTGTGCTTC CTCCTGGCAG CAACCAGATA GAGCTGAGTA 780 GCAGTCAGCC CCTTAGGTAA GGCATGGGCA CCCAGTTCTC CACAGTCCCC TACTTCCTGT 840 CCATCCTGAC ACGGAGGCCC TATGTCGGTT GCCATCTGTC ATCACATTCA CACTGTTCTT 900 AGTATAGAAA TGAAATTGGG GACATAGGAA AATGAAAGCT GTACCAAGAA GAGCTTGTGC 960 TTAAACTAGG CAAGAGCCTA TTTCTTTTTG GAAGTAGAGT GTTCGTGTGT GTTAAACATG 1020 TAATCAAGTA TGTCTGTGTC CAAAGACTAC AAGCCCCCCC CCAGGCCTGC CTGGCCCCGC 1080 AGGCATCTCT GTGGGTTACT TGGGCTGCGT TCTCCCACCT CAGTGACTGG ATTTAGCGTC 1140 TTTAGTTACC TCTTTAGGAT AAATGAACTG GATCTCAACA GAAGAGCCAG 1190
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