| Tag | Content |
|---|
EnhancerAtlas ID | HS007-16261 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr8:8167310-8168830 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPDEF | MA0686.1 | chr8:8167359-8167370 | ACCCGGATGTA | + | 6.62 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_35204 | chr8:8167172-8169264 | HeLa | | SE_36709 | chr8:8167342-8169158 | HMEC | | SE_38223 | chr8:8166974-8171370 | HUVEC | | SE_47375 | chr8:8166904-8175853 | Panc1 | | SE_65042 | chr8:8167194-8169201 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I008309 | chr8 | 8166880 | 8170979 |
|
Enhancer Sequence | TCCTCAGTGC TCAGCCCACA GGGATCTGTG AATGAAAATG AGACAGAGGA CCCGGATGTA 60
ATGCCACTTT CCGTTTGCTA AACTGAGTAG TGTCCATTTA CAGAAACACA GATACCCCGC 120
AGAGCCCAGC TGTGGCCATT ATCAGGGCTT GTATTATGCT CTTAACATCT CTGCAGGAAT 180
ATTCACTGTC TGTCTCCTGC ATTATTTCCT TTCCTTCCCA ATAACTTTAG AGTTACCACA 240
AGGGAAACAC TCCAGACCTC ACCAGGCCTG TCCAACTGAA GGTCATGATT CCAACCCTCC 300
ATCAAACTGC TACCAGAGGC CTGTGCCCCA GTGAAAAGCC GTTTTATGAG AGCACCTGTG 360
ACAGGTGTTG TTTAGAAATG GTTATCTTGG GCTGGATGTG GTGGCTCACA CCTCCAATCC 420
CAGCACTTTG GGTGATGGAG GTGGGAGGAT GGCTTGAAAC CAGGAGTTCT GGACCAGCCT 480
GGGCAACTTA GTGAGACCCC CATGTCTACA AAAAATTAGT CTGGTATGGT GGCATGAACA 540
TGCAGCCCCA GCTACTTGGA AGGCTGAAGT CGGAGGATCA CTTGAGCCCA GGAAGTCAAG 600
GCTGCAGTGA GCTATGATCA TACCACTGCA CTCCATCTGG GCAATGGAGC AAGGCTCTAT 660
CTCAGAAAAA AAAAAATAGA AGTGAATATC CTACCAAAAG AATGAATGAC TGCCATAGCC 720
ATTTAACATT GCCCTTGGTT TTCTTCATTT TGACTCTTTC TCCAATGAAC TGTTGCCTTT 780
TCAGAGATGA AACAAAGGGG GTAGTTGGGT AATAGGCCAG GGCCCAGCAG CTGGTTCCAG 840
TGAGGCCTGT CTGCAGGATG AACGCTGTGA TCAAATGTGT GACTCATAGT TGGGAGGTGT 900
CTGCCAACCC CGGCTGCAGG GCACAGTCGG CACTGACCGG GAAGGCAGGC TGATCTGCAC 960
CCTTGTCTGC TTCCTGTGCT GGGAGCGCAG CCCCCACCCC ACCTCATTCC CCCAACCCTA 1020
TCTCCACATG GAATTGTTCC ACTGGCTGTC ACCCAGGGAG CCCCTTCTTT CTACCCATGT 1080
TCAGTTGGGT ACTTGAAACA GCACATGACT CATGTTGTAC TCAGCCAAGA CTAACAGCAT 1140
CAGGCTTCTA TTGTTCAAGA GCTGACTCCA AGTTCCATGA ACTATTTCAA TGAGTGGAGT 1200
CCTTGTTGCT TACATTGCAG CTCTCTAAAG TCATGGAAAG AAATGACCAC ACTGGAGGCA 1260
CAGAAAAGCC AAGGCACAGA GTAGCACAAC CTTGCTCTTC CTTAAACACT ATCTCTGAAA 1320
GATCATCCTG AAGCATTTTC CTTGGAGAAC CGGCCATAGG CACCAGGTTG GGTTTGCCAC 1380
AAGGGACCAA TGCAGACCTT GTCAAAGAAG TGTTGAGTTG CAAGTGCAAA GACTAGCAGA 1440
GTCACTCCAG GGACTAGTAA GGGCCTGAGG GTGAATTTTA TCATTAACTC AGGGCTCTGC 1500
TGCCAATGTT AACTGCATTT 1520
|
