Tag | Content |
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EnhancerAtlas ID | HS047-07515 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:13053980-13055220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr12:13054975-13054992 | TGCTTTCTAGAAATCAT | + | 6.14 | Spz1 | MA0111.1 | chr12:13054353-13054364 | AGGGTAGCAGC | + | 6.02 | ZNF263 | MA0528.1 | chr12:13054320-13054341 | GAAGGAGGGTGGGAGGAAAGG | + | 6.98 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_02173 | chr12:13053863-13055157 | Aorta | SE_23547 | chr12:13053877-13054703 | Colon_Crypt_1 | SE_24533 | chr12:13054143-13054560 | Colon_Crypt_2 | SE_28138 | chr12:13053818-13055620 | Fetal_Intestine | SE_28922 | chr12:13051231-13057938 | Fetal_Intestine_Large | SE_34394 | chr12:13053736-13055358 | HCT-116 | SE_36163 | chr12:13051744-13055812 | HMEC | SE_38847 | chr12:13051287-13055917 | HUVEC | SE_57272 | chr12:13053856-13055846 | VACO_400 | SE_58021 | chr12:13053949-13054699 | VACO_9m | SE_64427 | chr12:13053735-13055819 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I012897 | chr12 | 13050309 | 13057779 |
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Enhancer Sequence | CATCCTTGTG TTACTGGATG GCTGTGTGTT AATTGTTAGC AGCTGGAATA AGTGAAGAGG 60 GTCTCGTCCT CATACTCAAA GTCCTTTGCT CATGCCCAAG GCCAGAGGCT ACTCATGCTG 120 AAACATTACC ATCTCCCTCC AAAGTGCAGG GTTTAGTCAC TGAGTACTGG GTGGAGCACA 180 TGACTGGATC CCAGTTAATC CCTCCCAGCT TACCAGTAAA ACCTCAGGAT TCATGCTTTC 240 CTGGGAGCCA CCTGCGGCCA CTAAGATAGG AGCGGGGTTC AGACATGGCC AGGCGCTCCT 300 AATCTCAGAC CCAAAGTGCA ATTTTTGGCA GCCTGCATGA GAAGGAGGGT GGGAGGAAAG 360 GTGGCTAGAA CCAAGGGTAG CAGCCTGGGG GCTTGAGAGG AAACCAGGCA CAGCCCATCC 420 TACCCTGTCT CACGAGCAGC CCGTCCTCCT CCTGACTCCC CTTACCCCAC ACACCGAGCG 480 CCATTCTCTT GCTGCCTCAT CTATTCTGGT TAGGTACTTA CTGAGCATCA GGTGCTAGGC 540 AAGTGGCTGG GGAGAGACAA CGTTTAATGA CTCAGTCTCC GCCTGCACAG AGCCTTTGAG 600 TCTAGAGGGA GACACAGACT TACTGACAGG CTGGGTTGTG TAATAAGTGC TACGGGAGGA 660 AAAGCTGAGA GTGTCTGAGA ATTTATGAGA TGTGTGTCTC ATCAGACTTG GGCATCAAAA 720 AAAAAAAAAA AAAAAAACCA TCCTGGAGGA AAGGACCTCT ACGTCAAGTG AAGGGTGGGG 780 TCCATTTGGT TTTTATAGGA GCAAGTTCTT TGTTGGCTGG ACTCTAGATC TCCCGTCCTT 840 TGACTTTGGT TACAAATAAT ATCCAAACCA CCGCTAGTCT CATTCTCTTT TCTCTTTCCT 900 GCTCTAGCCC TTTGCTCCTC TCCCAGGCTG TTTCTCTAGC TCCAGACAGT TCATATTCCT 960 AAATGCTGAT CACTTCTCTT TTCCCTCTCA AATGCTGCTT TCTAGAAATC ATTTTCAGTT 1020 TTTCAGAACC CTGTCCATCT CTTCCAATCC CCTGGTGTCT TTCCCTTACC TGGGTCATTC 1080 TCTGGGCAAC ATGGCACCCT TTCAGTGCAG ACTTGTTTAT TAATAACTCC AGTGAGTTTT 1140 ATTTTCCTCT TACTAAATTC AAAGTACTCA GAACATTTTA GACTTGTTGA GCAATCCCTA 1200 TCAGCTTAGG GATGGGGTGG GGGAGGCTAA CAGAGGTGAA 1240
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