| Tag | Content |
|---|
EnhancerAtlas ID | HS095-07801 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:110258090-110259970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr12:110258724-110258735 | ATTGCACAACA | + | 6.14 | | ZNF263 | MA0528.1 | chr12:110259255-110259276 | CCCTCCTGTTTCCCCTGCTCT | - | 6.17 | | ZNF263 | MA0528.1 | chr12:110259875-110259896 | GGAGGAGGAAGATAAAGGGCA | + | 6.57 | | ZNF263 | MA0528.1 | chr12:110259872-110259893 | GGAGGAGGAGGAAGATAAAGG | + | 7.93 | | ZNF263 | MA0528.1 | chr12:110259869-110259890 | GGAGGAGGAGGAGGAAGATAA | + | 8.14 | | ZNF263 | MA0528.1 | chr12:110259866-110259887 | TGAGGAGGAGGAGGAGGAAGA | + | 9.33 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I109820 | chr12 | 110258477 | 110259394 |
|
Enhancer Sequence | GATGAGATAC AGGGCTGAGC CAGGGTCCCC AGACCTTCCT TTCTGCCCTA GACAGAGACC 60
CCAGGCTTTC CAGAAACCTG GCTTTCTGCT CTCATGGCCC CCTGAGCCGG TGGGGCACAT 120
TTTGACGTCA GGCAGACCAG AGGGTCAGAT CCCAGACCCA CAGCTCACTT GCTGGGTGAG 180
TATGAGCAAG TTACCCAACC TCTCTGATCT TCACTTTCTT CAGCTGCCCT ATTTTTTTTT 240
TTTTTTTTTT TTTTTTGAGA CGGAGTCTCC CTCTGTCGCC TAGGCTGGAG TGCAGTGGCG 300
CATCTCCACT CACTGCAAGC TCCGCCTCCC GGGTTCACGC CATTCTTCTG CTCAGCCTCC 360
TGAGTAGCTG GGACTACAGG CACCCGCCAC CACGCCCGGC TAATTTTTTG TATTTTTTTA 420
GTACAGACGG GGTTTCATGG TGTTAGCCAG GATGGTCTCG ATCTCCTGAC CTCGTGATCC 480
GCCTGCCTCA GCCTCCCAAA GTGCTGGGAT TATAGGCGTG AGCCACTACG CCCGGCCCTC 540
AGCTGCCCTA TTAAGGGATC GTAATAGGGT CGTTGTGAGA GGTATATACC TTGAGTCAAG 600
TGCCTGGCAT AAAGAAAGCC TCAATAAACA GCAGATTGCA CAACAGATGG CTTCTCTCTG 660
AGAATCCCGG ATTCAAAGGC GGTGGAGGTC TCTGGCTCCG TCCCCATGCC CCAACTTGCG 720
GAGGGTGGAA AAAGGGGCCC ATCCTCGGGG TTACCCGCGG CTTTGCCTGA TCTCATGGAA 780
ACCCTGGCAA ACATTTGTCA AATCCCATCC TCCTGATTAC GTGACCAAGG AAAGCTGCTT 840
AAATCTGGGG GCAAGTTTGG GCATGCAAAC CTGCTCCGCC CCAGCGGGGA GGAATCCAGG 900
GAGCTGGTTT CTCCCGGTTC CCTCCCTTCT GGAATCAATT CATTCCACCA GGCATCAATG 960
CAGTGGCACC TGTTTGCAGG GCACAGGGGA GACATAAAAG TGTGGAACCT CAGAGAACTC 1020
GCAGTCCAGG AGGGAAGGCT GATGGCTCTC TCTGCCTCCA GGCCTTTGCC TAGGCTGTTC 1080
CCTCCGCCTG GAATGCCCTT CCCTTCGCTG GCTGGCTCCC ACTTACTCCT CAGGCCTCAT 1140
GTTAAAGGGC ACTTCCTCTG AAAAGCCCTC CTGTTTCCCC TGCTCTTTAC TCTTAGAGTA 1200
ACATGTGCCT TCCTTTACAG CACTTCCCAC GATTAAACTT TTCTATATAT GTATTTTTTT 1260
TTTCAAGAGA GTCTCGCTCT GTCCCCCAGG TTGGAGTGCA GTGGCATGAT CTCAGCTCAC 1320
TGCAACCTCC GCCTCCTGGG TTCAAGCAAT TCTCGTGCCT CAGCCTCCTC GAGTAGCTGG 1380
GATTACAGGC ATGCACCACA ACACCCGGCT AATTTTTCGT ATTTTTAGTA GAGGCAGGGT 1440
TTTGCCATGT TGGTCAGTCT GGTCTTGAAC CCCTGACCTC AGATGATCCA CCTGCCTCAG 1500
CCTCCCAAAA TGTTGGGATT ATAGGTGTGA GCCACCGCAC CCGGCCTATA TATTATTCTT 1560
TGATTCATCT TCTCTCTTCA CCTCCAGAGT TTTAGTTCCA TGTGGTAGGG ACTATTTCGT 1620
GTCCCCTGTG TCCCCAGCAT TCAGCATGGT GCTGAAGCAA AATGAGGTGT CAATGAATAT 1680
TTGGTTTTTT TAGGCTGTAA GATCAGGGAC CTGAAGTTCC AGGCAGGGTT GCAGAGCAAG 1740
GGCAGCCAGA ATCCTGATGG GGAGGGGGAA AGGCTGTGAG GAGGAGGAGG AGGAAGATAA 1800
AGGGCAGAGG AGGTGTCAAG GACAAAGGTG TAGAGGGGAA AGTGCAGGGT GCACAGAGGA 1860
ATGGTGTGGC CTGGGGCACA 1880
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