Tag | Content |
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EnhancerAtlas ID | HS034-22966 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr4:74977410-74978640 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr4:74977630-74977645 | CCATGGACCAATCAG | + | 6.98 | RREB1 | MA0073.1 | chr4:74977965-74977985 | ACACAACACACCCCCATCCT | + | 6.4 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_34020 | chr4:74973468-74984340 | HCC1954 | SE_34944 | chr4:74973434-74984043 | HeLa | SE_35924 | chr4:74973407-74984079 | HMEC | SE_38660 | chr4:74973379-74978167 | HUVEC | SE_46049 | chr4:74973285-74983971 | Osteoblasts | SE_55844 | chr4:74970769-74984442 | u87 | SE_64715 | chr4:74973303-74981674 | NHEK | SE_67651 | chr4:74970769-74984442 | u87 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH04I074107 | chr4 | 74973459 | 74983803 |
|
Enhancer Sequence | GACCTGGAAA TAGCTGGTCA CATTGGCTAT ATTGATAGCA ACAGGAGATA GACAAATTCT 60 TAGGCAGACA GGGATGCGTC CCTGGTAAAA CCTGATCTCC AAGCCAAAGA CAGCCTGAAG 120 ACTGAAAACT GAGCTGCCAG TTCGGGGTAG AGCCCATGAC CAGAGTGAGA ATTTCCTCGA 180 TGCCTTTTAG CCAATATAAT GATGCTTTTT CCAGGCCCAC CCATGGACCA ATCAGCATAC 240 ACTCCCCCAT TCTGAACCCA TAAAAACCCC AAACTCAGCC TTACAGACAG CCACCTGCTT 300 TTGGGCCTCC TCTCACACAG AGGACCATCC ACTTCAAGTC CCCTCTTGTG TTGAGAGCTT 360 TTCTGCCACT CAGGAAAATT CTTCTCTGCT TTGCTCACTC TCCGGTGTCT GTGTACGTCA 420 TTCTTCTTGG TCACAGGACA AGAACCCGGA ACATGCCAAA AGGGTGTAAC ACATACTCCT 480 GCTCACTGAG TTACAGGAGT GAAAAAAACC ACTGGGTGCC GCATGCCCCT ATTTAGCAGG 540 TACAAATGAG CTGTAACACA ACACACCCCC ATCCTCCAAG CTGCAGGCAG CAGGGAGAGC 600 TGTAACATGC CTCCATCCTC CGAGCTGCAG GCTCAAAGAA GTGAAGCAGT TAGGCACTAT 660 TCCCTCCTGG CCAGCTTGCT GAACTACAAA AGCTGCAACA TTTCTTGGGA GCTTAGACCT 720 CAGGATTCCC CAGGCGAGAG CTGTAACATC ACCTGGGGCT CCACAGTTGC TGGCATCTCT 780 GAGTTTTCAG GTGCCACTGC ATTCCCCTCA TCTAGACTCC GGCTCCCAAT GCAAAAGCTG 840 CCTGTGGCAT GCCAAGTTTA GCCACAGGCA AAACACAGAG TCCCTGTTCA GATGTGGGAT 900 CCAAGCAGGT AGCACAAGCT GAGTACAGCC CATCAGGCTG AGTGGGAAGA GTGAGCCCAG 960 CAGGCCTTGG CAAGACTACA GGCAGAGGTC ACAGCAGCCA CAGAGATTTC CAGCTGGTGA 1020 AGCAGCACTG AAGGAGTCCT GTAACAGTAT GTTAGTCTAC AAACTTGGTA AATTCTCATT 1080 CTCTGTTTTC TGTGACATTT TGATTTTAAA AATTTTATTC TCCAATACAT CGCAAGGACT 1140 GGATATCTTG CCCTCTATTT TGAAAGTATG GTGTCCAAAT TCATAGGAGA AGGCAAGGGT 1200 AGGTGACTCA GAAGGCACAC ACACCAAAAA 1230
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