| Tag | Content |
|---|
EnhancerAtlas ID | HS197-20200 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr7:139930320-139932170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr7:139931456-139931477 | GGGGGAGGGCAGAGGTGAGGA | + | 6.32 | | ZNF263 | MA0528.1 | chr7:139931441-139931462 | GGGGAAGGGAGGACAGGGGGA | + | 6.3 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_10688 | chr7:139928670-139933684 | CD19_Primary | | SE_23582 | chr7:139928853-139932390 | Colon_Crypt_1 | | SE_23882 | chr7:139929232-139932362 | Colon_Crypt_2 | | SE_32404 | chr7:139929315-139932427 | Gastric | | SE_35628 | chr7:139928783-139932537 | HepG2 | | SE_50458 | chr7:139928716-139934014 | Sigmoid_Colon | | SE_52813 | chr7:139928906-139934034 | Small_Intestine | | SE_58244 | chr7:139929339-139931797 | VACO_9m | | SE_58244 | chr7:139931837-139932241 | VACO_9m | | SE_63142 | chr7:139906757-139942538 | Tonsil |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I140229 | chr7 | 139928803 | 139934470 |
|
Enhancer Sequence | CTGCCCCCCG GCGCACTCTC GCCGCCCCGG GGTCCGAAGC ACCGCGCACT CCACCCCGCG 60
ACGCGCGCAT CCCTCGACCC TCGCGCGTCC ACACCGCCGC TGCGCCTCGC GCCCCCGCAC 120
CCCCGCAACC CCACACCACG CCGGCCGGGC GGGGCCGGAT GCGCAGACGT GCAGCACGTG 180
CGCTGCGCAG CGATTGGCAG CGCCGCCCCC ACGCCGCCCC GCCAGGGAAA GGGTGTCCCG 240
TGCCCTGCCG CGGCTGCTGG TCCCGCGGGC GGGGGCTGTC GGGGCGCGCG GGCCGGGCCG 300
TGGGGGTCGC CGCCCGAAGT GACCGGGGAA CAATGACAGC CCGATGGGGA AGGGCGGCGG 360
CTTCCCTAGA GGGCCGGTTC TCTGGCTCGG AGCTGGGGGG CGTGGGGGCC GTAGGTGTTG 420
CTTCTGCGGA ATGGAAATAC TTTCTGTGAG TGGTGCGCAC GTGTTTCCAC TTTATTTGGT 480
TGTCAACTGG GGCCCAGTGC ACTTAAACCC AGCGTTATTC GGGACCGAGC CAGGAGATCA 540
CTGCACCCTT CAATCTGCGG GTGGGGGGAG GAGTTAGGAA GGGGACTGAG TGACAAAAGT 600
GACAGAGGCG CAGCTCATGT GCGTGACCGG GGGAGTGATG CTCAGTTCTG GGTGGGGGAC 660
CAGAAAGATG TCCACTGCGG GACTGGGCGA TGAAGGGGCG GATTTGAGTG GCGGCTACTG 720
TTTCCCGGCC TGGGACGGCT GCCGGGCGGG CAGGATCTGC AGGCGCGCGG CCGGGACGCG 780
CAGGGAGCGC GCAGGGAGCG CGCAGGGAGC AGTGGGGCTT CCCGGGCCGC TTCGGGGAGG 840
TGGGCAGGAA AGGGCACGCA GCCCTAAGTG ACTCTCGGCT GAGACTGCCT CTCCTCATCC 900
CAGCAGTAGC CAGCCAATGA AAAATAGGCT CAGGGGGTTC CCGAGCCAAT GGAAGCCCGC 960
GGGCCGTGAG GACTTGCCAC TAGAAACGTT TATGGTGTCC CGGCCCGGAG ACTTCTGTGT 1020
GTTTGTTAGG CGGGGCGGGG GGCGTCTTCC CAGCAGCCCA GGACAGGTGT GTGCCCAGGC 1080
GGATTAGAGC GCCTGCTGTT GGTAAGGCCC CTGCCGTGGA GGGGGAAGGG AGGACAGGGG 1140
GAGGGCAGAG GTGAGGAATC TAGGAGCTGG CGAACGGTTT CTCCCGCTTT CTGTGTCCTG 1200
CGTCACTTTC CCTTCTGTAA ACGGTGGTCT TCCCTTTGTG TCGTGTTTGA TCGTTTCTAA 1260
ATTGCTTTCC CATGCATTAC TTTACCCAGC CATCACTGTA ACCCACAAGA TGGGTTTGAT 1320
TACTCATTTT ACCAGCAGGG GAAGTGAGGC TCAGGTAAGT TAAATCCTAG GCACATGGTG 1380
GCACAGCTGC TTAGTACAGG TTTGGGACTG GAACTCAGGT GCCCCGACGA CAAATCCAGG 1440
GCTCTTTAAC TACATCAAAG GAAGGAAACC AGGTCTGTTT TATGATCCTG GTGCCAAGGG 1500
CACACCCAGT GATTAAACTG AAATCCAGAA GGACCGGGTG AGTTTTATTT CCCCTTCAGT 1560
CATGCTCTTT CAGGTTGTCC CTTTGCAACA CAGGTTTGCT CTGCTATTAC ACGCCATGCC 1620
TTAAGATTAA GAGAGTTCAC TGACTGCCAG AAAAGCCAGA AGTAAAAAAA CAGAATGTGT 1680
GTAGGGGCGG GCGGGTTACC CACTGTGCAT TTCCTCCTTA CCCACACCCT CAGGCCAACT 1740
CGAGACCCGT GGTCCTCTCT CATGTTGGTC CCCCACCTGC AGATACTGTT TCCTGTTCCA 1800
TGGACTGGGC TCGGCCTGCC TAAAATAGGC TGCACCCAAG AAGCTTCTAC 1850
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