| Tag | Content |
|---|
EnhancerAtlas ID | HS102-05599 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr12:13144880-13146830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:13146079-13146097 | CCTTCCTTCCTTCCTTCC | - | 10.83 | | EWSR1-FLI1 | MA0149.1 | chr12:13146083-13146101 | CCTTCCTTCCTTCCTTCC | - | 10.83 | | EWSR1-FLI1 | MA0149.1 | chr12:13146058-13146076 | CCCTCCCTCCCTCCCTCC | - | 6.03 | | EWSR1-FLI1 | MA0149.1 | chr12:13146062-13146080 | CCCTCCCTCCCTCCCTCC | - | 6.03 | | EWSR1-FLI1 | MA0149.1 | chr12:13146091-13146109 | CCTTCCTTCCTCTCTCTC | - | 6.25 | | EWSR1-FLI1 | MA0149.1 | chr12:13146067-13146085 | CCTCCCTCCCTCCCTTCC | - | 7.08 | | EWSR1-FLI1 | MA0149.1 | chr12:13146071-13146089 | CCTCCCTCCCTTCCTTCC | - | 8.13 | | EWSR1-FLI1 | MA0149.1 | chr12:13146087-13146105 | CCTTCCTTCCTTCCTCTC | - | 8.32 | | EWSR1-FLI1 | MA0149.1 | chr12:13146075-13146093 | CCTCCCTTCCTTCCTTCC | - | 9.42 | | IRF1 | MA0050.2 | chr12:13145885-13145906 | ATGGTGAAACTGAAACAAAAA | - | 6.81 | | Nfe2l2 | MA0150.2 | chr12:13145562-13145577 | TGCTGAATCATTCTG | - | 6.78 | | ZNF263 | MA0528.1 | chr12:13146083-13146104 | CCTTCCTTCCTTCCTTCCTCT | - | 6.58 | | ZNF263 | MA0528.1 | chr12:13146075-13146096 | CCTCCCTTCCTTCCTTCCTTC | - | 6.76 | | ZNF263 | MA0528.1 | chr12:13146079-13146100 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | | ZNF263 | MA0528.1 | chr12:13146062-13146083 | CCCTCCCTCCCTCCCTCCCTT | - | 7.05 | | ZNF263 | MA0528.1 | chr12:13146071-13146092 | CCTCCCTCCCTTCCTTCCTTC | - | 7.19 | | ZNF263 | MA0528.1 | chr12:13146054-13146075 | TTCCCCCTCCCTCCCTCCCTC | - | 7.32 | | ZNF263 | MA0528.1 | chr12:13146067-13146088 | CCTCCCTCCCTCCCTTCCTTC | - | 7.38 | | ZNF263 | MA0528.1 | chr12:13146058-13146079 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_46589 | chr12:13143937-13147247 | Osteoblasts |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 13145446 | 13145954 | | chr12 | 13145478 | 13145960 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I012990 | chr12 | 13143372 | 13147333 |
|
Enhancer Sequence | AGCTTTACAT GTGAGAAGTG CAACAGATAT TTATTTGATT AAGGTGCTGT GTCTCCTAAC 60
AATGATTATG AAAAACAGAC ACATGGTAGG GAACCTGGCT GCCCTAGACT GGTCAAATAG 120
GTTTTCATAT AATATCCTAG ACTGAAGATT CACAACTAGG GAAGAGGGTG TGACTCCCAG 180
GGGGACAGAA GGTGTCTCTG GAGGAAGGCA GGACTGTACG GCTGTGAGTG GCAAGTGTAG 240
TCTCAATGAG CATATTTAAT ATTTATTTTA TTTTTGAGAC AGAGTCTTGC TCTGTCACCC 300
GGGCTGGAGT GCAGTGGTGT GATCTCTGCT AAGAGCAACC TTCACCCCCC AGGTTCAAGT 360
GATTCTTCTG CCTCAGCCTC ACAAGTAGCT GAGACTACAG GCGAACGCCA CCACTCCCAG 420
CTAATTTTTG TGTTTTTAGT AGAGATGGGG TTTTGCCACA TTGGACAGAC TGGTCTCGAA 480
CTCCTGACCT CAGGTGTTCT GCCCACCTCG GCCTCCCAAA GTGCTGGGAT TACAGGTATG 540
AGCCACTGTG CCCGGCCTTA ATATTGTAAT TTTAACCCTG AGTGCCAAGT TTGTACTTAA 600
ATCCCCCTTC ACATGGGGTA GAGGAAATTG CGCCAGACCA GGAATCATGA GGCAGCAAGT 660
CAGCCTTGAC TGTGGGGCAC CGTGCTGAAT CATTCTGAGG CTGCTGTGAA GCCCTCCATC 720
TGGTGAATCT GACACTTCCA AAGAGCCTTC AGTAGCAAAC TGTTAAGTAA ACTTAGGGTG 780
TTTTGCTCTT TCTGTTGCTG CAGAGAATTC CAGAACTCCC CTTTCATTTG AGAGCGCACC 840
TACCCTTGGC ACTTGTAATG TTTTAAATTC CAGAAACACT ATCCTGTGAA TCACAGAAGT 900
TCAGAACCTA AAATGGTTTT AAAGTTTACC TAATCTAACT AATTTTATCA AGGAGAAAAT 960
GAAGAACCAG AGAGACTAAG TTGCTCAAAG TGATGTAACT ACTGAATGGT GAAACTGAAA 1020
CAAAAATTCC AGTTCCCAAA CTCTAGTCTA CTCCAGTCTA ATACTCGTTG CAAGGTTCTC 1080
TAAAGCTATG GGGGGTGAAG TGAGCATTTA AACCTCTGTT TCTTTTCTTT ATCCTCCTTT 1140
CTTTCCTCTC TCTGTCTTTC TTTTTTTCTT TCGTTTCCCC CTCCCTCCCT CCCTCCCTCC 1200
CTTCCTTCCT TCCTTCCTTC CTCTCTCTCT CTCTCTTTCT TTCTCTTTCT TACAGGGTCT 1260
CATGGTTGCT CAAGCTGGAG TGCAGTGGTA CAATCTTGGC TCACTGTAAC TTCAGCCTCC 1320
TGGGCTCACG TGATCCTCCC ACCTCATCCT CCTAAGTAGC TGGGACTACA GGTGTGTGCC 1380
ACCATGCCCA GCTAATTTTT TTTGTATTTT GTTTTCTCTG TCTTCTTTTG TAGAGACAGG 1440
GTTTCACCAC GTTGCCCAAG CTGGTCTCAA ACTTCTGAGC TCATGCGATC CACCTATGTC 1500
AGCCTTCCAA AGTGTCTTTG CTTTTTTTTT TTTTCTTTTC CTCTCTCTCT CTCTCTCTCT 1560
CTCTCTCTCT CTTTCAGATG GGGTCTTGCA ATGTTGCCCA GTCTGTAACC TCTCTCTTTA 1620
GCCACTGTGT TAGATACTTT GGGCGGACAG TTGTATGCCC ATATCAAATT CAGAATAGAG 1680
GTATCAGAAG TCATTTTACG CAGTTACTTC TTTTACAAAT GGGAAGACCA AAAACAAGAT 1740
CTCACTGGAG AAAGAGCTAA CTGGCTCTTT CCTTTGGTCT TTTTCTTCTT TTATTCATTT 1800
AACCAACAAC TACTGAGTAT CTACCATGTG CTGAACATTG TTACAGGTGC TATAAGGGAA 1860
GATGCCAGGA AAACAGAATG TTATCATCTA ATGATATTTT TAGGGGGCAA GGAGTGCCAG 1920
GGCAGTATGG GAACACAGGA AAGGACCACT 1950
|
