Tag | Content |
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EnhancerAtlas ID | HS148-03888 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr12:12901920-12903010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr12:12902415-12902426 | AACCAATCAGA | + | 6.62 | NFYA | MA0060.3 | chr12:12902486-12902497 | TCTGATTGGTT | - | 6.62 | NFYB | MA0502.1 | chr12:12902487-12902502 | CTGATTGGTTGCTTT | - | 6.7 | SOX10 | MA0442.2 | chr12:12902777-12902788 | TTCTTTGTTTT | - | 6.62 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_07055 | chr12:12901996-12903340 | Brain_Hippocampus_Middle_150 | SE_23308 | chr12:12902361-12903081 | Colon_Crypt_1 | SE_24059 | chr12:12902412-12902755 | Colon_Crypt_2 | SE_25894 | chr12:12902004-12903177 | Duodenum_Smooth_Muscle | SE_31618 | chr12:12902443-12902794 | Gastric | SE_45697 | chr12:12900270-12903960 | Osteoblasts | SE_52464 | chr12:12902262-12903017 | Small_Intestine | SE_53337 | chr12:12902294-12902978 | Spleen | SE_56035 | chr12:12901815-12903298 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I012748 | chr12 | 12901735 | 12903167 |
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Enhancer Sequence | GTAAGTGTGA GGTGCACAGT GCTGAAATTA ACCTGTGACC AGGAGATTTC TACTAACTGG 60 GTTTAAATTC ACAGGCCATG GGGTCTGTAC TCTTGGCATT GATCAAGTGG CATTTTGGTG 120 AGGCTGCAGT CTCTGCAACA GTCTTTGGGC ACCCAAAGCA CTGATTCTGG GTATGCGATT 180 CTGCTTGAGC TACCTGCTAG GAATTGGCTT ATTTTATGAA GATGGCTGGG ATAGAGCCAG 240 TGCTATGATC ATTTTACATG TTCTGTTAAA TCTATAGATT CTTTAGAAAA AAGTACATCC 300 CAGACTAGGC TGATATTGAG GCAGGAGAAT AGGGTCTGGA AACAGGGAAC CTAAGGTCAT 360 TTCACGCTAA CTTTCTAGAA CTAAATTTAA AGAAAAACCC TAACATTCCA CGCCTAAGTA 420 ACAAAAGGAC CAGAGGCTAC TCCCTTTGCA AACCCCCACC TTTTCTGCCC AGCAGATGGG 480 CAATTGGCTG TCAGCAACCA ATCAGACTGA TTGCAGGCAG AGTCTTAGTT TCCATAGAAG 540 TGCAACTTTG TAACTTCACC TTAACCTCTG ATTGGTTGCT TTTTGCAGCC AATTAGTTGT 600 TTGCACAGGA GTGTGACGTT GGTAACTTCA GCCTCTAATT GGTGGCTTTC CGCCACCAAT 660 CAGAGCAACT GCGGACCACC ACTTTATTTA CATGAGGTGA CCACCAAGTG GCCCATGGGA 720 AACCTGTAGG GGGTATTTGG ACCCAACAGA ATTCTGTAAC CCGGGTTTTT GAGCCGCTGC 780 TCAGGCCGCT CCCACACTGT GGAGTGTACT TTCGTTTTCA ATAAATCCCT GCTTTCATTC 840 TTTAGTTGCT TCATTCTTTC TTTGTTTTGC TGGGCATTTT GTCCAATTAT TTGTTCAAAA 900 CGCCAAGAAC TTGGACAACT TGCAGTCAAG ACCCTCTACT AGTAACAATA TTATCATTAT 960 TTTTTGACTT GGAGGCCCTG AAGGAAATGC CCCCATTCCA ATGAAATACA GCTTAAGCTG 1020 TACTTGTCAA AAGATCCCTG ACTGTACCCC CACACTGAAA TCCCTTCCGG TAGAGACAAA 1080 GCATAATAAG 1090
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