| Tag | Content |
|---|
EnhancerAtlas ID | HS147-01526 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:53124090-53126470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:53124701-53124721 | GTGGTGGTGGTGGTGTGTGT | - | 6.27 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_11041 | chr1:53123809-53126983 | CD20 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I052658 | chr1 | 53124521 | 53124670 | | GH01I052659 | chr1 | 53124738 | 53126336 |
|
Enhancer Sequence | ATAACAGTAA ACTATGTAAT ACTGAACAAC TCTGGAGCCA AATGCCTGGT TAAAATCCTG 60
CCCCTGTCAC TTACTTGCTA GGTAACCTCT GTGCCTCAGT CCTCTCATCT ATATAAGCTG 120
GAATCTTAGT AGTATCTTCT AATAGGGCTT GGGGAAGGAC TAAATTACTA AGTCCATGCA 180
AGTACATAGA AAAGTGTTGG CAAATGGAAA GCACTATGTG TTAGCTATTA TTATTATTTT 240
TAACATGTCT TATTATTAAT CTGATCGCAA AGGAATCTTA GGGCAAGATG CTGACTGTCA 300
GCCCTCCCTC CTGGCTGCTC TCCTAACTTT GGCGATGGCT TTTAGGCTTC GCCTTCGGAA 360
TGCAAGACAA GGACTGTGGA GACGCAGCTC AGCAGCCACC AAAAGCAGCT CTTGACATTT 420
CAGACAGTGA CATGACCTGC TGCTGGATTT GGCAACAGTG AAAGAGTCAC TCTTAGATAC 480
CTGTGCCTGA GGCCAGCCAA AGGGTACATG ATGGGGTGGC AAGACAGGGT GAGTCACCCA 540
CAGAAGTGTT CTAGGCTGGA AGTCAAGAGA TTTTGGTTCT GGTCTTGCTT CATTTGTTGT 600
TGTTGGTGGT GGTGGTGGTG GTGGTGTGTG TGTGTGTGTG TGTGCTCTTT TATTTCAGCA 660
TTTTTTTTTT GAGACAGTCT CATTCTGTCA CCAGGCTGGA GTGCAGTGGA GATCATAGCT 720
CACTGCAACC TCAAACTCCT GACACAAGCA ATCCTTCTGC CTCAGCCTCC CAAGCAACTG 780
TGACTACAGG TGCGTGCCAC TGTGTCCAGC TAATTTTTAA ATTTTTTTTT TATCGAGACG 840
GGTGGTTGCT ATGTTGCCTA GGCTAGCCTT GAACGTGTTG GGATTACAGG TGTGAGCCAC 900
TGCACCCAGC CTATTTTCAG CACTTAAAAC CCAGCACCCT TGTCCATTTA CTGCACACTT 960
AGTGGTATCC ATTCTATTCT AGGACCTGTG CAGGTTGCCA CAAACAAGAG GAATCAGACA 1020
GTTCTCACCC TCAAGGGGCT CACATGGAGG ACAAGGCAGG CACACAAATG GCCAGGAGGC 1080
CCAGTGGTGG CCCTTCATGG GGCTTTAGGG AGGAAGAAAT GATGTCTGAG CTGAATCATC 1140
AAAGATGACT CAAAGTTTCC AGGTGAGACA GGAACAGAAA ACATTATGGT CAGAATACAG 1200
CTTGTTCACA ATAGTGAGAG CGAGCCAGTG TGGCCCAGGA CCTGCAAGTT ATTTGTTATA 1260
GAAAGAGCTT AGGGTACTTG TATATATGTG GTGGGGCTGG GTGATATTGG GATGTTTAGT 1320
CCCTGACGCT CTGTGCGACC CTTCACAGGA CGAATTCCTT CTCTGTCCTT GGTATCCTCA 1380
TCAGAAAAAT CCAACTTTTC TCTGAACACT TTCAAGGGAG ACTGGGAGGT TTCAGGAAAG 1440
AATCTGATAA TGCCCTTGCC TTTAGGCTGC TAGCAGTCAG AAGGGGGAGA TGCTGTGTGC 1500
ATTCCAAACG CTAAAGTGGT CATCCGCGGC CTAAGGCAGT GGTTCTCAAA CTCGAGGCTG 1560
CATCAGAATC AGCTGTGTGG AGGGCTTGTT AAAACACAGA ATGCTGGCCT CCTACCCCAG 1620
TGTCTGACTC AGTAGGTCAG GAGTAAGTCC CCAGAATTTG CATTTCTAAC AAATTCCAGG 1680
TGATGCTGAT GATGCTGGTC TGAGACCACC CTTTGAGCAC AACAGCCTCT GCAAGAACAA 1740
AAACAAGCTT TGAGGACTCC GAGCCAGAGA GATGTGGGGG AGACCGCACA CTGAGCAAGG 1800
CCCTGAAGAC CTGGTAGAAT TTCCCCAACA GTTGGAGAAA GGGAATGTAC ATGCTGCTTT 1860
TGCTGACCTA CACATCCTAG GCCTCATAAA GCCCCTCCCT GCCCCCCAAC AGCTCCTCTC 1920
CTTTGAATTC AATCAAGGCT CAGAGCCGGC TGTCACTGGG GTTGGCTAGT CTGGGTCCTG 1980
CATTAGAAAC AAACTGCCCA CCCTGTGTGA TAGGAGCCCC TCCCCCAGGG CAGCCGCAGT 2040
GGGAGGATGC TGGGTGGGCT GATACGCAGA CAGAAATAGT CTGAGCTCAC CGCTGTTCCC 2100
AAGCACACAT CGACCGGCAA TTATTTCTTG TAAATTGCTT TCCCGGTTAT GTTCAGAACA 2160
TGTGTGTGTG CCTGCCTGAG AACAAACACT CAGAGGGCAC AGGGCGGAGG AGCTAGCTGG 2220
AGAGTGGGCT TCGGATGGAG GGGAGTGAAT CTTCAGCCCA GAATTAGAGA ATGTTGAATC 2280
TTGGAACTTG GAAACGTTAG AACATTCCAC TCCCCTTTAC AGCTATCCTG CTAGGTGTTT 2340
TTTTCTCAGA CGTTCACATT TGTTTGTCCA TTCAACATTG 2380
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