| Tag | Content |
|---|
EnhancerAtlas ID | HS129-24471 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr22:45999650-46001890 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
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 | chr22:46000791-46000811 | ACACACACCACACACACACA | + | 6.16 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_35224 | chr22:45997208-46002928 | HeLa | | SE_56446 | chr22:45995854-46001776 | u87 | | SE_67937 | chr22:45995854-46001776 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I045602 | chr22 | 45998221 | 46001953 |
|
Enhancer Sequence | GCTGCCTGTT TTTTTTTTTT ATTCCTAAGG GACATCTATT CTACTGTACA GAGGAAGTCT 60
GTGGCATGTG TCAGAAGTGC CTGGGCTGCC CAGGGTCCTA GCAGGACCCG TTTTAACATG 120
CAGGTGGGCA TTGAGTGGAG GGTGCCAGGG CCCACCCAGC CAACCCAGCC AAGCCAGCCA 180
ACTAGAATTC GAGGAGGTAA GCCAGCTTTT CCAAAGTTCT CAAGTTTGTC CAGGTGAAAA 240
AACACCTGGA AATCAAGGGT TTTTTTCCTA ATATTGTAAC ATGAAAATTT TCAAATATAC 300
AGCCGAGTTG AAGGAATTTT ACAGTGAATA CCAGGGCACC TTCCACCTAG ATTCTGCCAC 360
TGACATTTTA TGAGATTCAG TTGCATTTTG AAGAAATGAC AATATGATGA ATTAATAAAT 420
ACAAATAAGA AACTTACAGT TTCTTGTAGG CTTGCGCTCA AATCCAGCCA CTTACTAGCT 480
GTGTGTCCTT GGGCACATTG CTTAATGTCT CAGAGCCTTG GTTTTCTCTA CAACGAAATG 540
AAAATAAGGA CACATACTTC ACAGGAGTGA TTGTTAGGAT GAAAGGGGAT GATTACGTAA 600
AACAGTGCAA GAACTGCTAC ACAGGAGGTC CTCCATAAAT AGTACTGTCA TGACACACAC 660
ACCCGAAAGG ATAGTCTTTA TTCAGTTAGA TGCCACATTT TATTAAAGTC TTGTGTGGAC 720
AAGAAGTGAA ACCTCAGAGG AATTTATGAA GAATAATTGG AGGCACTTCC TTGTGACTTG 780
GCTTCATCCG GACCGGATGA CTTCTGGGTG CCAGCAACAG TTCCCCATTT CCATTCACGT 840
TTCCCCACAT CGTTCATGCC AAAGAGATGG GTGCCAAGAG GCCATCCGTC TTCATCCTGG 900
ACATAGAATG AGACGGGAAC TCACTCTTGA AGGACTTTTG AAGTCTCAGA GAAGAAACGG 960
AGCCACCGTA GACCTTTTGA AATACGGCCT GTGAGAAGCA CGGTGACAGT CACCATTACT 1020
ACCAATAATC ACATTACTCT TTGTGGGAAA AAAGACCTAC TATGTGCCAG GAAGGCTTCG 1080
GTAATCATCT CCAACACACA CACATTCTCT CACACACACA TGTGCGCATG TGTGCACACA 1140
CACACACACC ACACACACAC ACACACACAC TCCGCAGCCC TTCTGCCATG CCCAGCTCAG 1200
GGCCATCTTC TCCCACAAGG ATGCCGGTCT CATCTCCTGA AATGAGGTTG CAGTGAGCCG 1260
AGATTGAGCC ACTGCACTCC AGCCTGGGTG ACAGAGCGAG ACTCCATATA ACCTCTGCCT 1320
CCTGGGTTCA AGAAACTCTT GTGCCTCAGC CTCCCAAGTA GCTGGGATTA CAAGCGCGTA 1380
CCACCACACC CAGCTAATAT TTTTTGTATT TTTTAGTAGA GACAGGGTTT CGTCATGTTG 1440
GCCAGGCTGG TCTCGAACTC CCAACCTCAG GTGATCTGCC TGCCTCAGCC TCCCAAAGTG 1500
CTGGGATTAC AGGCATGAGC CACCGCGCCC GGCCTGATCT CAGTCTTTAA GAGAGCAGCA 1560
GCTCATCTGT GGCCACTGCT TCCCAGGGAC TTGCCAGAAG GGAGGTGCAG GGCACAGGGA 1620
AATAACCCAC CTCTATCTGA CGGCTTCAAT GGTATCGAAT GTCCTCAGTG GCAGCACGCA 1680
GCACAGAAGC TGAGGTGTGG CTGCATTCCA TTTGGAGAAT TCCACTGTGA TTCATGGTGT 1740
CAGCTGCGGG TTCAAGGTGT CACAATTTAA TTATTAAACA TCATGAGGCA TTAGGAGGCT 1800
TGGGCACGCA CTGATAAGTG ATCCATTTCT AACACAGCTG GTTTATTACT GTTTGTGGCA 1860
GCTCCTGCAC GAATTGGTGT CCGTTAACTA AGCAATGGTA TTATAATTAC ACATTTAAAT 1920
TATGTATGGG AAGGGTGTCA GTGGTAGAAG TCAGACTGCA GTGATTACTT TCAGTCTTCA 1980
GACCTCCTGG ATGTAGTCTC TCTGCAGATA GCTGTAACTC TGGCTTGTTT TCTGCTCATT 2040
TTCTGCAGAC ATGTAGAATC CACTGCTAGG GTCCACTGAG CTGTCTTCTG GGTGGTTTTT 2100
GGTGCTGCAG GAGATAAACA CATGTGTCTT CCTGGTTGGA CCCAGTTGAT GCACTAACCT 2160
AATTCTGTCC TTTGCCTGCC CTGATCTCCA TAGCCTGCTT CTTCCTGGAA ATTTGCTGCT 2220
GCTGCTGCTT CTTTTTTTTT 2240
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