Tag | Content |
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EnhancerAtlas ID | HS034-26170 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr6:42282020-42283480 |
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) |
ESR2 | MA0258.2 | chr6:42283288-42283303 | AGGTCACCCTAACCT | + | 6.71 | Klf1 | MA0493.1 | chr6:42282551-42282562 | AGGGTGTGGCT | - | 6.02 | PPARG | MA0066.1 | chr6:42283285-42283305 | ACGAGGTCACCCTAACCTAA | - | 6.07 | RREB1 | MA0073.1 | chr6:42283446-42283466 | CCCCCCCCCACCCACTGCCA | + | 6.66 | ZNF740 | MA0753.2 | chr6:42283441-42283454 | CCACCCCCCCCCC | + | 6.44 | ZNF740 | MA0753.2 | chr6:42283444-42283457 | CCCCCCCCCCCAC | + | 6.92 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09954 | chr6:42280232-42287506 | CD14 | SE_53138 | chr6:42280173-42285189 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I042312 | chr6 | 42279850 | 42286337 |
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Enhancer Sequence | TAAACATCTC TATTCACAAG AAAACATGCT TTAGAGTATG AGTCTACCCT GATCGAACTC 60 TTCATCAACA TAAATCCCTG GTTTTACAAC AAGAAGCCAA GCTCACCCGA TGCTTTCAAA 120 TGTGCACAGT TAAACTAGGG CAGAGGTCCC AGCAAGCCTT GCAAAATTAA GCTCATGCAT 180 CTAAAAAAAT ACTGGCCGAG TGCCTCAATG CTAGGCATTG TTCTCCGTGA CTGGCACGCA 240 ACAGTGAACA AAGAAGACAA AACTCCCTGC CCTCATGGAG ATTTCATTTT AATAGGGAGA 300 AACAGAAAAT AAAAATTATT ATAATTAAAG TGTATAGTGT ATTAGATGGC TGTAGATGCT 360 ATGGGAAAAA ACAAAGTAGG AAATAGTCAG GGAAGCCCTC TCTGAGAAGG TGACATCTGA 420 GCAAATGCCT GAAGGAATAA GAACAATGAG ATCTGGGGAA AGAGCATTCT AGGAGGAGGA 480 ACAGCAAGAG CCCTGTGGTG GGTACATGCC GGATGTGACT GAGGAATTAG AAGGGTGTGG 540 CTGGGACAGT GAAAACCAGG AGGAAAGCAG TAGGAACAAG GTCAGAGATT CTAAACGTGA 600 TTTTAAAACA AAACAGAAGT ATAAACTTGA TGGAGCGAAT AGGTTGGTCG CATAGGGTGC 660 TTAGGAAAGG CCAAGGTAAG GAGGTGTCAG TTGAGCTGAG ACCTAAATGA GCAAAGCATG 720 AAGATGTGAG GAGAGAACGT TCACAGCAGT GGTGACAGCG AGTGCAGTGG CTCTGGCAGG 780 GATGAGCGTG CATGTGGCAG GTGTGCAGTG GGTGGGATGA GGCAGCGTGG TAGGACGGGG 840 TCTCCATTAT GTAGGGTAGT GGTCTCCACC TGGAGTGATT TTGCCTTCCA GAGGACATTT 900 GGCAGTGTCT AGAAACATTT CTGTGTCACG ACTAGGGAAG TGCTATTGGC ACCTGGTGGG 960 CAGAGATGCT GCTAAACATC TTACAATGTG CAGGACAGTC CCTTTCAAGA CAGAATTCAC 1020 TAGCTCCAAA TGTCAATAGC ACTAAGGTTG ACAAACCCTG GTGCAGGGCC TCACAAGTCA 1080 CAGTAAGAAG TCTGGGTGCT CACAGAAGCA CATGCCAAGG ACTTTCTAAT GCCTCGTGCC 1140 TGCTGGAGTG TGATCCTTAC ACGTGGCACA TCCAGGTCTA GAGTATGGCA CATTGGGATG 1200 AAAGAGAAGG GCGCTAGGAT CGGCGCTTAG AGCACAGAAG CAGGGGTAGA GGCAAAGAGG 1260 CTGTGACGAG GTCACCCTAA CCTAACTTGG AGCTAAGAGG GAGCTCCTGG AGTAGAGACA 1320 AAGGAGGTCA AATGAAGGGG GGCCATCGGG CTGTCTTCTA GCAGCTGATA TCCTTCAAGA 1380 GACCAGGTGG GGCCCCTGGG TCAGGGTTGG GGAGAGGAAC ACCACCCCCC CCCCCACCCA 1440 CTGCCACCCC CTAACGTCAT 1460
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