| Tag | Content |
|---|
EnhancerAtlas ID | HS105-17707 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:13144810-13146990 |
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 | TGGTAATGAA ACATTATTAT AGTTTTAACA ATCTGCAATA AAGCCTTTAT GGGCAGAAAC 60
TATACCACAG AGCTTTACAT GTGAGAAGTG CAACAGATAT TTATTTGATT AAGGTGCTGT 120
GTCTCCTAAC AATGATTATG AAAAACAGAC ACATGGTAGG GAACCTGGCT GCCCTAGACT 180
GGTCAAATAG GTTTTCATAT AATATCCTAG ACTGAAGATT CACAACTAGG GAAGAGGGTG 240
TGACTCCCAG GGGGACAGAA GGTGTCTCTG GAGGAAGGCA GGACTGTACG GCTGTGAGTG 300
GCAAGTGTAG TCTCAATGAG CATATTTAAT ATTTATTTTA TTTTTGAGAC AGAGTCTTGC 360
TCTGTCACCC GGGCTGGAGT GCAGTGGTGT GATCTCTGCT AAGAGCAACC TTCACCCCCC 420
AGGTTCAAGT GATTCTTCTG CCTCAGCCTC ACAAGTAGCT GAGACTACAG GCGAACGCCA 480
CCACTCCCAG CTAATTTTTG TGTTTTTAGT AGAGATGGGG TTTTGCCACA TTGGACAGAC 540
TGGTCTCGAA CTCCTGACCT CAGGTGTTCT GCCCACCTCG GCCTCCCAAA GTGCTGGGAT 600
TACAGGTATG AGCCACTGTG CCCGGCCTTA ATATTGTAAT TTTAACCCTG AGTGCCAAGT 660
TTGTACTTAA ATCCCCCTTC ACATGGGGTA GAGGAAATTG CGCCAGACCA GGAATCATGA 720
GGCAGCAAGT CAGCCTTGAC TGTGGGGCAC CGTGCTGAAT CATTCTGAGG CTGCTGTGAA 780
GCCCTCCATC TGGTGAATCT GACACTTCCA AAGAGCCTTC AGTAGCAAAC TGTTAAGTAA 840
ACTTAGGGTG TTTTGCTCTT TCTGTTGCTG CAGAGAATTC CAGAACTCCC CTTTCATTTG 900
AGAGCGCACC TACCCTTGGC ACTTGTAATG TTTTAAATTC CAGAAACACT ATCCTGTGAA 960
TCACAGAAGT TCAGAACCTA AAATGGTTTT AAAGTTTACC TAATCTAACT AATTTTATCA 1020
AGGAGAAAAT GAAGAACCAG AGAGACTAAG TTGCTCAAAG TGATGTAACT ACTGAATGGT 1080
GAAACTGAAA CAAAAATTCC AGTTCCCAAA CTCTAGTCTA CTCCAGTCTA ATACTCGTTG 1140
CAAGGTTCTC TAAAGCTATG GGGGGTGAAG TGAGCATTTA AACCTCTGTT TCTTTTCTTT 1200
ATCCTCCTTT CTTTCCTCTC TCTGTCTTTC TTTTTTTCTT TCGTTTCCCC CTCCCTCCCT 1260
CCCTCCCTCC CTTCCTTCCT TCCTTCCTTC CTCTCTCTCT CTCTCTTTCT TTCTCTTTCT 1320
TACAGGGTCT CATGGTTGCT CAAGCTGGAG TGCAGTGGTA CAATCTTGGC TCACTGTAAC 1380
TTCAGCCTCC TGGGCTCACG TGATCCTCCC ACCTCATCCT CCTAAGTAGC TGGGACTACA 1440
GGTGTGTGCC ACCATGCCCA GCTAATTTTT TTTGTATTTT GTTTTCTCTG TCTTCTTTTG 1500
TAGAGACAGG GTTTCACCAC GTTGCCCAAG CTGGTCTCAA ACTTCTGAGC TCATGCGATC 1560
CACCTATGTC AGCCTTCCAA AGTGTCTTTG CTTTTTTTTT TTTTCTTTTC CTCTCTCTCT 1620
CTCTCTCTCT CTCTCTCTCT CTTTCAGATG GGGTCTTGCA ATGTTGCCCA GTCTGTAACC 1680
TCTCTCTTTA GCCACTGTGT TAGATACTTT GGGCGGACAG TTGTATGCCC ATATCAAATT 1740
CAGAATAGAG GTATCAGAAG TCATTTTACG CAGTTACTTC TTTTACAAAT GGGAAGACCA 1800
AAAACAAGAT CTCACTGGAG AAAGAGCTAA CTGGCTCTTT CCTTTGGTCT TTTTCTTCTT 1860
TTATTCATTT AACCAACAAC TACTGAGTAT CTACCATGTG CTGAACATTG TTACAGGTGC 1920
TATAAGGGAA GATGCCAGGA AAACAGAATG TTATCATCTA ATGATATTTT TAGGGGGCAA 1980
GGAGTGCCAG GGCAGTATGG GAACACAGGA AAGGACCACT TAGGTTAGTT TATGGGGCAT 2040
GGGTGTATGT GATAACATGT TTGGGGAGGT CAAGCTGACT TTGAGGTGGT CACAGATCAC 2100
CCAACCGGAC GTTCAGTCAC TACTTTATTA ATTCATGGAA TAAACATTGT CGAAAACCTT 2160
TGCCAGGTGG TACAGATTTG 2180
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