Tag | Content |
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EnhancerAtlas ID | HS176-38143 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:104607200-104608680 |
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) |
GATA2 | MA0036.3 | chr7:104608392-104608403 | TTCTTATCTTC | + | 6.02 | ZNF263 | MA0528.1 | chr7:104608031-104608052 | GAGGAAGGAAGGGGAGAAAAG | + | 6.05 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_44335 | chr7:104607173-104609136 | NHDF-Ad | SE_44865 | chr7:104607604-104608389 | NHLF | SE_45643 | chr7:104607292-104609597 | Osteoblasts | SE_49374 | chr7:104607703-104608608 | Right_Atrium | SE_54878 | chr7:104607395-104608574 | Stomach_Smooth_Muscle |
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| Number: 2 | ID | Chromosome | Start | End |
GH07I104967 | chr7 | 104607662 | 104608086 | GH07I104968 | chr7 | 104608110 | 104608364 |
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Enhancer Sequence | CCCGGCCAGA GATGACCAGT TTTCTGATGA ATGGTGTCCA AAGGCTAGGC CCAGACCCAA 60 GGCCTGTAGG GAGGCAGTAT AGCTGAGATC TGCACAGTCC CTTCGACAAA CATACCATGT 120 GTGGGATAGA TGAAGGGGCA AAGGAACCTT GAGAACCCTT GGCCAGTGAT TAAGAGTATT 180 TACCTGGCAT CAGAAAGATC TAGTCTAGGT TCAACTTAAA GCTGTGCTAT TTACTCTTTG 240 CGTGACCTTG AGCAAGTCAA CCTCTCCCAG CCTCAGTTTC TCCAAGTGTT GTGGTCATAA 300 TTAAATGAAT TTAAGTACTG ATGTACTTAA GACAGTTCCT GAGACAGACT GAGCTCTTAA 360 CTGCCATTAA TTACTGCTAT CGATGTGAAT ATTCGAGCAG CACCAGCTGA TGGGAAGGAG 420 GAGGATCCAG GATTGGGTGG GTGGGTGACA GCAAGCAGGG AACTAACCTG GCTGGCTAGA 480 CTGGCCTGGG AAAGGTAACC AGGTGGGCTG AGTAGATAAG GCAAGCTGGG ATCTGGTTCA 540 GTTGATTATC AGTATCTTCA GGGAGCAAAG TAAGCAGCTG GAATGACTGT GAGAGAGTGG 600 GGATAGTAGA CCAAAGTCAG GAAGGAGTCA TGGCTCTTGA GCAATTGACT TAATCCAAGC 660 AGAGCCCCAG CCAGTAGGGA CTGAGGAAGG TTGGAGAGGA AAGTATATTG GCAAAGAGGA 720 AGACAGGGTG ATTGAATCCC AGCTGACAGG CGGAGTCCAG TCCTAATAAG GGAAACTGAG 780 GCACAAGGGC ATCCTAATGA ACTAGGTCAC TGCAAAGTGG ACTGTCCAAT AGAGGAAGGA 840 AGGGGAGAAA AGGCTGTGAT GAGGTAAACC TTGAACTCTC AGAGCTCTGT TGTAGCCCAG 900 GAGATAATTA CCAGCCTGCT AGGCCTGGCA GGGTCGGTGG GGCTGAGCCT TCCGAAGTTC 960 TTTCTAGAGC AGTCATGGTC ACCAGTGACT CGAGCCAGTT TACTCCCCTC TTGCACCCAG 1020 CCACTCAATC AGAGTGCAAA CTGCCCGATG CCAGACCACA GCTCCTAGCA ATGTGATAAT 1080 CTGGTGCCCA GGAATGTGAG AATGGTCAGT GCACAGGAAT CTGAGGCAGA GAGGATATAT 1140 GGTGACCACT CCTCAACAGT GGCAAGAGCC TGTACTTGGA AGAAAAGGAT TTTTCTTATC 1200 TTCCTAGGAC AAACCTGTAC TTTGTTACTA GAAGAGAGCT CCTGGGTTTG CCCGAGCTGT 1260 CTGCTCAGGT TTTTTTTCTT TTTGGAAACA GTTTCGTTCT TGTTGCCCAG GCTGGAGTGC 1320 AATATGGCAA GATCTTGGCT CATCACAACC TCCACCTCCT GGGTTCAAGT GATTCTCCTG 1380 CCTCAGCCTC CTGAGTAGCT GGGATTACAG GTGCCTGCCA CCACGCCCAG TTAATTTTTT 1440 GTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGGCCAGG 1480
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