Tag | Content |
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EnhancerAtlas ID | HS141-17396 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr7:101371000-101373120 |
Target genes | |
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) |
Klf1 | MA0493.1 | chr7:101372912-101372923 | GGCCACACCCT | + | 6.32 | MYC | MA0147.3 | chr7:101371485-101371497 | GCCCACGTGCTC | + | 6.27 | Nr2f6(var.2) | MA0728.1 | chr7:101371841-101371856 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr7:101371017-101371038 | GGAGGAGGAAAGGGAAAAAGC | + | 6.88 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_10104 | chr7:101370825-101373861 | CD14 | SE_29361 | chr7:101370592-101374033 | Fetal_Intestine_Large | SE_56546 | chr7:101369926-101374393 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I101727 | chr7 | 101370998 | 101373711 |
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Enhancer Sequence | ATCAGCCTCT GGCCCTGGGA GGAGGAAAGG GAAAAAGCAA GTTAGGGGAT GGGACTGTAG 60 TCGCAGCTCA GAGGCCCTGG GTGCCTCTGA CACTGAGGCA GAAACAAGGG GGAGCATTAG 120 CTGGATTTCT ATCCTACACG TGTCAGCGGA CGTGATGGTT TCAAACTGAA AGTGAGCAAT 180 TTGTGGGTCC TTGGGCCACA CCTATGAAAG GCTTTTTTAT TTTTTATTTT TTGAGACAGG 240 GTCTGGCCAG CTATTTTGTT GTTGTTGTTG TGGAGATGGG GTTTCACTAT GTTGCCCAGG 300 CTGGTCTCGA ACTCCTGGCT TCAAACGATC CTTCTGCCTC TGCCTCCCAA AGCACTGGGA 360 TTCGAAAGGC CTTTTATGTG AAACACTTGT GACCCACCAA AAATCCCATT GTAAGTCCTG 420 TCGCTCTGAC AAGCATCATA ATCGCGCATC TGTCCAGAAT TCTGCATTTA GGAGGAGGCT 480 TTAAAGCCCA CGTGCTCAGA GCTACGGTGT AGACCCTATA CTCCACCATC CTGCCACAGG 540 ATTCAGGGAG CAGCTGGAGG TAAGATAATT GTAGGCTCCA GGCTCTGCAC CCTGGGTGGG 600 ATTAGCATTA GTCAGTAGGT TTCTCTGTTC CCTCAATCTC CCCGCTCCCG GGACTTGCAA 660 AGCAGTGAGA GTGGGCAACA TGCCGTGTAA CACAGTTAAT TACACGTTGA TTGCATTGTG 720 CTGTAATTAC TGTTCAGGCG TGTGGGGCTC CTCACCTGCA CTGGATCCTG GAACTCAGAG 780 AAAGAAGCTT CTGTCTCCTG TAATCCCAGC ACTTTGGGAG GCTGAGGTGG GCAGATCGCT 840 TGAGGTCAGG AGTTCAAGAC AAGCCTGGGC AACATAGCGA AACCCTATCT CTACTAAAAA 900 TACAAAAATT AGCCGGGCGT GATGGCAGGT GCCTGTAATC CCAGCTACTC GGGAGGCTGA 960 GGCAGGAGAA TCGCTTGAAC TCGGGAGGAG GAGGTTGCAG TGAGCCGAGA TGCCACCAGT 1020 GCACTCCAGC CTGGGTGACA GAGCGAGACC CTGTCTCAAA AAAAAAATTA AAAAAAAAAT 1080 TAAAATTATA ATAAAAATAA AATTGATTGT AGAAATTGCA CTAATGGATA CATTAGAAGC 1140 CATTGAATTG TATATTTTTA ATGGATGAAT TGCATGGTAT GTGAATTATA TCTCAATAAA 1200 GCTATTACTT AAACAGGAGA AAACAAAAAA CCCCAGCGAC AATCTTCCTC AAGCTCCTTG 1260 GCAATAGGAG GCCTTGCCGT CCCCACCCAG CCTGCCTGAG TTCCTGCTTA CAGTTGCTTC 1320 TTTTTTTTTT TTCCTTTGAC ACGGGGTCTC CCTCTGTCAC CCAGGCTGGA GTGCAGTGGC 1380 GCAATCTCAT CTCACTGCAA TCTCCACCTC CCGGGTTCAA GTGATTCTCC TGCCTCAGCT 1440 TCCTGAGTAG TTGGGATTAC AGGCACCTGC CATCATGCCC GGCTAATTTT TGTATTTTTA 1500 TAGAGATGGG GTTTTACCAT GTTGGTCATG CTGGTCTTCA ACTCCTGACC TCAAGTGATC 1560 TGCCTGCCTT GGCCTCCCAA AGTGCTGGGA TTACAGACGT TAGCCACTGC TCTCAGCTGC 1620 TTCTTAAATG CGGCTGGGGC CAAGCAGAAA AATGGCCCTC TCTCATGCTA GGCAAACGCA 1680 GAGCCCACTG GACAGAGTTC CCTGAGATCG AGGCAGGGAT GACGCATGGC TGCCTTGTGA 1740 CCAGCTATCT CTCCGCTCTC TGGTGAACTA TCCCAAGCCA GACCGTGGTT TTGTAATTTG 1800 AAGTCCAAGG CCGTGAATCA ACATAATCTA CTTATCAAGA CCAAAGGCTG CGGTCGCCGT 1860 GCATGTAGAA GGAATAGCTC ACAGTGCGTG GCGCCTTCAT GCCGGAGGGC TGGGCCACAC 1920 CCTGGTGCAC ACTGGGGGTG GTGCCCAAGG ATCCTGCTGG ACTAACCAAA CACAGCCCTG 1980 GGCCACACCT TCCCACAGGC CTCTCAGCCC TCTCAGCTCT TCCACTTGGA GCCTGAGAGT 2040 CTGACACCCC CCACCTCACC CCCAGTCAGC TCTGTGACTC CCAGTGCTCT GGCTTTGGGA 2100 TTTGTTTTGT TTATTTTAGA 2120
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