| Tag | Content |
|---|
EnhancerAtlas ID | HS147-14952 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr15:51384320-51386740 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr15:51385298-51385309 | AAATCTCAGCA | + | 6.32 | | ZNF263 | MA0528.1 | chr15:51385079-51385100 | TCCTCCTCCCGCTTCTCCCTC | - | 6.81 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_38708 | chr15:51385309-51391596 | HUVEC |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I051092 | chr15 | 51384798 | 51384997 |
|
Enhancer Sequence | TCTTATGGCA GGGCTTTTTC ATAAATTCAG GAAATGGAAA GGCATGGATG AGGAAGCAGC 60
CCTTATGTCT CAACTCCCTG TGAGGCAGGT ACACACACAC ATATAAGTAC TCCAAGAGGT 120
CCCACTCACT CTGCTGTACT TCTCAGTTAC ACCCATTCAG CTTTCATAGA TACAGGTCCA 180
TGGATGAATG TCAAGTTTCT TGTAGAGACA AAGGTCAATC TCTAAGGAGA ACACACCTGT 240
TATCTAACCT GTATCTGAAT CTGCAACAAC GGTTTCCATT TGACAGGATG CAGCCCTAGC 300
AAGGTGGTGA ATTAACATCC AGCTTTGAAG CACTGTCATA CAGGAGAATA CTTTAAGATG 360
GAATATAATG CGTGAGACTG ACTGCCATTT AGCAGAATGG CTTGTGACAT TAAAATACAT 420
GTTCAACGTG TGAGATTCAA GCACACGCAG AAAGAAGAAA CAACTGCAGA AAACAGTAAG 480
GTGCAAACAA ATAGTGACAG CTCACGAGAG CTGTCTGCCC TGTTCTTCAT GGGGCCCATC 540
TGACCTTAGT GATGTTTGCT GTCAGCTACG CAGAGGCCTT CTGACACAAA CTGACCGTGA 600
ATACAACAGG GATATTAAAC ACTGGGTCAG GCTGGAGAGA GAAAACAACA GGGTGCAGCA 660
GAATTCTTTT CCTTCCCTTT CACCCAAGTA CCAGGGATTC TGAAGATTCT CCTCCCTGCC 720
CCCGGCTTCT CTTCCTTCCT CTTTCTCTAA GCCTCCTTAT CCTCCTCCCG CTTCTCCCTC 780
AACCCCTTAA CTTCAACCAG AAGAAGAGAT AGAGGGTTGG GCAGGGGAGC ACAGAGAATG 840
TTGTTCTTAG GATTTTGAGA GAGTTAAGCG TCAGGGTCAA TGTCCCCTTC CCGCTTGCGC 900
TCTCGAAATA GATACACACA AAACATCTAC TGGAACTTTT AAATGATGAG AGGAGATCCA 960
CAAGTCACCT GTGAAGCAAA ATCTCAGCAC TTTATAGTCA CAGAAACATA CAGGCATGCA 1020
AAGGGCTCAT GTTTATGAAT TATATCATAC CTAGGCAAAG CAGGTGGCAC TTGCACACAC 1080
ACAGGAATCC TTAAATACAC GCATCTTGGC ATTTCCTTTC CGCCAGCCTT GGCCCTTCCC 1140
ACCCACCCAA AGGTGCGGGC CACAGCCACC CTCTGTGGGG TCTGATGCAG GGTGAAGGGC 1200
GTCACTGGGT CCTGGCTACT CCCTGGCTGT GAGAAGTGGG CAAGCCCTTT ACTCTATGGG 1260
AATCTCTGTA AAATGAAAAT AACTGCCTGG CCAGGGGCTG TGAGGATGAA AGGGTATTAA 1320
TAATATACGC AGGGCACTGT CCTGCTTGGT TCCCGAACCT CTCTTTCCTA CACCCACGGC 1380
TGGACTGATG GTGCCTTCTG TTACTTGGTC CCCACCGTCA GTACTCTAGT GTGACACTGG 1440
GAAGAGTGGG GGCTTAGCCA GGGCCGCGGT CTGTACAGGA GGGTCCCAGC CCGCAGGTCA 1500
CGGGTCTGCA GGCCCACAGC TAACCTTCAG AGCTGCACAA GCGCCGGGAG CTGTGGGCAC 1560
GTGAGGAGGG CGAGCGGGTC CTAGGTGCGT AGACCCGTGG GTGGGGGGCG GAGCGGACCG 1620
GTGGAGGTGG GCAGAGACCG GCGGCAAGTC GACCCACGGC TGTGGGTGGC TTCCTCCTGT 1680
TGCTCAGTAT CAGGGAGAGG CGGGGGAGGA CATTCATTTT TTTTCTTCCC TAAGTAAGCA 1740
TCCACCTATT GCTTTAATAA CTATCGATTG TGAAAAGCCG GCGGGGCCTC TTAAAGGCGA 1800
AGTCGGGAGG CGCGCGCCCC TGCGTCTGTG TTCGGGGACC AGTCCGCGGG GACCTTCTGG 1860
ACCTTCTCCG CCGGCTGCGC GGCAGCGATG GACCCTGTGC ATGGGCTCTC CTAGCAGCCT 1920
CGGGAACCGC GGCCGCAAGC TGTGGTTTGA CCCCTGCCCC AACCACTCGC GAGGCCTTTT 1980
CTGTTCAGAG CCCCCAGTCA CGTTCTTGGA CCCAGTCACC TGCGCCGCAG CGCAGTCCCG 2040
GCGCCCCAGG TTCGAGGACC CGGCCCGCGC TCGGAAAGTT ATTTCAAAAG GCAGATGTGT 2100
TGCAACCCTC TCTGCAGCAA ACTACAGTAC GCGGATTCCC GAACCCTTCC CCGCCCCCAC 2160
CCAGCCCGGG CGACCAGAGC CCGCCGCGGG AGACTGGCAG CAAGGAGAGC CACCCCTAAA 2220
TGCACCTTCC CTCCCTCCCG CGCGCCCAAG TGCAATGGGG TTGGGGGAAG CCCCAAAGCA 2280
AACTCACGAC GCGGAGCAAT CCCCAGTCTT GGCCTGGAAG GGGTCGGGCT GCTGAGGATC 2340
GGCTTCCCGA TTTCATGCCC CAGCCTCCCG TCCTCCCCAG CCCCAGCCCA CCCGCCTGGG 2400
CCGTCGCGGC CCCTAGGTAC 2420
|
