Tag | Content |
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EnhancerAtlas ID | HS095-05016 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:15814140-15815490 |
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) |
HES2 | MA0616.2 | chr11:15815394-15815404 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr11:15815394-15815404 | GGCACGTGCC | - | 6.02 | RARA(var.2) | MA0730.1 | chr11:15815321-15815338 | AGGTCACCGTAAGCTCA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_46521 | chr11:15813620-15816493 | Osteoblasts |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I015792 | chr11 | 15813709 | 15816085 |
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Enhancer Sequence | GAAGGACTTT ACAGTTATTA TACATTAATA AGACAGAAGA CCTTTCTTTC CTTTCTTTGA 60 ACTATTTTGT CCAATTTAAA TCATGTACTA GGGGTCACCT TAATAAATTA CAGGATTTAA 120 GAAAGAACAT GGAGATCACA TCCTTGATTT GAACTTTGCC TTGAGACCAT AATATAATAA 180 GCTTTTGTTG CTTGACATGT TTCCAGTTTA ACTTTTATAT GTTAAATACA AGAATCTGTT 240 ACAACCTACA GATTCTGAAA GTTCAAGACT CTCTTTTTCT TTTTATTCTT GCTTTAAAAC 300 TAGCCATGTC CTTCTGAACT CATCTCTTCT TTATAGTATC TTGTCATATC CTTTTATGAA 360 CAACTAAGTC ACACATGCCT CATCCCACTG GCCAACCTTA TCACCTAAAG CCACTGCTTC 420 ATTAGATAAA TTATCTGTCT TGCAAGTTAT CTTATGGTTT TACAAATGTT TAGTTATTTC 480 CTAATGTGAG TCATAATGTT ATCAGATTCA ATAATAGTTT CCTCACTACC CACTGCTTGA 540 CTCTGAAGCT AGTTACATAA TTTTGTTGTT TTTGTTTTGT TTTGTTATGG TAACACCCCA 600 CTTCTGGTAC AACTTCTGTA TTAGTCAGCT TTTACTGAGT ACAATCATAG TAACTCCCTA 660 AAGTCTCAGT GGCTCCTAAA CATAAAATTT AAGTTTGCTC ATATGTAATG TGAGCCTTAC 720 CTAATGACAG CTGACTTATA CACTTATGCA CTGGGACTGT AAGTTCCAAA GGAAGGCCTC 780 AGTGCTTCAG AGATGGTATT ATAGTAACCA GGAAATCCGA CAAGAGGGAA GAAACTTTCT 840 CCTTCTGCTG CTTTTCTTAA TACAGTGAAT GACTTCACCA TCTATCTAGC TTCCCAAAGC 900 TACAAATAGA TAGATGAGTA ATCCTCTATT TCTTCCTCTC CTTCACCCCC TACACTCTCC 960 AGTCATCAAG TAAAAACATT CCTGGCAACT AGAACATTAC CTGACTCATT GTGTAGTCCC 1020 TCTAAACGTT TGCTGTTTTT ATGTTAATGC ACAAAAATAT ATGATCAAAA AATATATAAA 1080 GTTTATGAAA TCCCTATTCT AAAGCAGGGC CTATTTTTAT TTTTTTTTTA GAGAAAGGCT 1140 CTTGCTCTGT TGCCCAAGCT GGAGTGTACT GCCACAACCA TAGGTCACCG TAAGCTCAAA 1200 CTCCTGGGCT CAAGTGATCC TTCCACCTCA ACCTCCTGAG TAGCTACTAC TATAGGCACG 1260 TGCCACCATA CCTGGCTAAT TATTTTATTT TATTTTTTTT GTACAGATGG CGTCTTGCTA 1320 TGTTGTCTAA GCTGTACTCA AACTCCTGGC 1350
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