| Tag | Content |
|---|
EnhancerAtlas ID | HS176-10094 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr12:89763800-89765550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr12:89764028-89764040 | TCTAAAAATAAA | + | 6.07 | | MEF2C | MA0497.1 | chr12:89764026-89764041 | TATCTAAAAATAAAA | + | 6.26 | | ZNF263 | MA0528.1 | chr12:89764384-89764405 | CTCCCTCCTCCCTCTTCCCTC | - | 6.11 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_25078 | chr12:89763202-89764109 | Colon_Crypt_3 | | SE_27644 | chr12:89763300-89771362 | Fetal_Intestine | | SE_28566 | chr12:89761572-89775819 | Fetal_Intestine_Large | | SE_35929 | chr12:89761762-89771214 | HMEC | | SE_38298 | chr12:89761862-89771214 | HUVEC | | SE_50215 | chr12:89763222-89765656 | Sigmoid_Colon |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I089368 | chr12 | 89761900 | 89775589 |
|
Enhancer Sequence | CCCCGAGGCC AGAGGGTGGT GCGTTCAGGT AGCAAAGACA GGTGGGCTCC GTCCCGCCTT 60
CACCTGCAGC TGCCCTGGCT GCTGGTGGAG AAAATATGAC AAATTCTAAT TTTTCTGCAC 120
ATTAATGTGC TGTGGTATAG GTCTAAGGGA GGGGGCGCAG ATGGTGGTGA TGGAAGTGGA 180
AACAAAAAAA TCAATGAAAG AGACTCTTGA TAAAACAAGC GTCATATATC TAAAAATAAA 240
ATAATAACAA ATGGTTATCC TAGCGTATAC ATCCAGATGA CATTTGGAAA TTTGCATAGA 300
AGTAACAGAA GGGCTAAATG AAGCCTTCTG GAAAAGTCAT AGTCTTTCAA ACTTTATGTA 360
CTCTTGGATT CTAGAAACTC ACTTCAGTTA TTTAAGTGAA ATGACCAGAA TTAGTGTCAT 420
CTCCATACAT TGAGCAGGAA GTTAACTTTG AGGAACTATA CATGAGCACT TGTCCCTGAG 480
GTTGTAGTAT CTTTATGTCC TTTCCACGCC CTCGCCACAA AAAGCCCCAG CAAGAACAAT 540
CAATGTTTTC CTGCTTAACC CGTATTTTTA TCTGAATGTA CATTCTCCCT CCTCCCTCTT 600
CCCTCTAGGC ATTTGCTAGG CCCTTAGGAG GTCAGGCAAC TTGCACTGTG GCACATGAAG 660
AATATTCACA TACTTCATAT CCTGCAGGAG AAAGGAGACA GCACAAGAAA TTCTGTTGTC 720
ACTAATTGAA AGTAGTTTAT CACTTTATCT TTAGAAGGTC TAATGCCAAA ACTTCAAGGA 780
GATAATAAAT AGTCCAGTCT GGGTTTGAGC CTGGAGTTTG GATGTCTAAG ATGACTCCGA 840
GCGGATGTGG ATTTACGTGT TAGTACCTGA AAGTGGGCAC AGCCCCCACC TTGGAATGAA 900
TGTACACTTC CAAAGGACTC GTTCCCACAG GGTGGTGGAA GGAACAACAG AGACAGCTAT 960
GTGCCCACAT GCTCAGCCAT CTGCCATTCC AACCACATGT CTCTCCCCCC GTTTCCTGCA 1020
AATGATTCAT CTATTCTTTT TCTCCTTCTT CAAAGATAAC TCTGTAAGCA CTTAAGGAGG 1080
GGAAAGTCAT TAAGAAAAGT GGAATCTGGA GTTATTAGGA TGAGATAGAG CAGATTAAAC 1140
AGTCTGGAAT TTCACAAAGC AAACAGCACA GGGTGCGGAC CCTGGGCCCG TCTCTCTCCT 1200
GCTGGTGCAT CATTTCACAG GTTATCATCC TTCATGAACA GGTCAACAAA AATGGCCACA 1260
GGTAAACATG AGCATATGAG TTGCTAAAGA GAAAGAAAGA CAGAGAACAG CAGAAGTCAG 1320
GAGGATTCTG GATTTTCCAA CTGGAGCCTC TGTGCATCTT ATCCAGCATC ACAGACAGTG 1380
TCTGTCGCTA AGTGATGCCA AAGGTTTTAC ACCAATGAAT GGGATCTTTG TGACGTTTTC 1440
CCAATAACAG ACCAAAAAGC TGCCACTAAA ATCATGCTTT TAAAGGAGAT CCTGAACAAT 1500
AGCCAGTGAA GGTGATTATG GCCATGTCCC CATGTCCATG AGGAGGTGCT TGGTGGGTAT 1560
TTGTTGAATT GCATCAAACT GGAGTTGGAT GGGACTCAGT TCAAATCCTG ACTCTGCTTC 1620
CAGCTTCTGG TACATTAGGC AAGTTGCTAA ACCTCTGGGC TTAGGGGATA AAGACACTAC 1680
CTCACAGGGT GGAGTGAGGA GTAGAAGATA ATATACGTGA AGTACTTCAT GTGGTCTTTG 1740
GAAAGAGGTA 1750
|
