| Tag | Content |
|---|
EnhancerAtlas ID | HS098-29466 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:30877560-30880440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:30879875-30879893 | TCTTCCTTCCTTCCTTCC | - | 10.05 | | EWSR1-FLI1 | MA0149.1 | chr2:30879871-30879889 | TTTCTCTTCCTTCCTTCC | - | 6.22 | | EWSR1-FLI1 | MA0149.1 | chr2:30879891-30879909 | CCTCCCTTCCTCCCTTCT | - | 6.66 | | EWSR1-FLI1 | MA0149.1 | chr2:30879887-30879905 | CCTTCCTCCCTTCCTCCC | - | 8.37 | | EWSR1-FLI1 | MA0149.1 | chr2:30879879-30879897 | CCTTCCTTCCTTCCTCCC | - | 9.47 | | EWSR1-FLI1 | MA0149.1 | chr2:30879883-30879901 | CCTTCCTTCCTCCCTTCC | - | 9.6 | | ZNF263 | MA0528.1 | chr2:30879896-30879917 | CTTCCTCCCTTCTCCTCTTCC | - | 6.06 | | ZNF263 | MA0528.1 | chr2:30877597-30877618 | CCTCCCCTCTCCTCCTCTTCA | - | 6.12 | | ZNF263 | MA0528.1 | chr2:30879878-30879899 | TCCTTCCTTCCTTCCTCCCTT | - | 6.28 | | ZNF263 | MA0528.1 | chr2:30879893-30879914 | TCCCTTCCTCCCTTCTCCTCT | - | 6.31 | | ZNF263 | MA0528.1 | chr2:30878976-30878997 | CCTTCCTTCCCCTCCTTTTCC | - | 6.3 | | ZNF263 | MA0528.1 | chr2:30879886-30879907 | TCCTTCCTCCCTTCCTCCCTT | - | 6.66 | | ZNF263 | MA0528.1 | chr2:30877606-30877627 | TCCTCCTCTTCAGCTTCCTCC | - | 6.81 | | ZNF263 | MA0528.1 | chr2:30879899-30879920 | CCTCCCTTCTCCTCTTCCTCT | - | 7.38 | | ZNF263 | MA0528.1 | chr2:30879890-30879911 | TCCTCCCTTCCTCCCTTCTCC | - | 7.44 | | ZNF263 | MA0528.1 | chr2:30879875-30879896 | TCTTCCTTCCTTCCTTCCTCC | - | 7.52 | | ZNF263 | MA0528.1 | chr2:30879883-30879904 | CCTTCCTTCCTCCCTTCCTCC | - | 7.61 | | ZNF263 | MA0528.1 | chr2:30877594-30877615 | TCCCCTCCCCTCTCCTCCTCT | - | 7.95 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_02790 | chr2:30877917-30879757 | Astrocytes | | SE_37388 | chr2:30876077-30880796 | HSMMtube | | SE_64142 | chr2:30877473-30880186 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I030654 | chr2 | 30877580 | 30880446 |
|
Enhancer Sequence | CGGTCTTTCT CTCCCACCAC ACAGTGAGCT TAAGTCCCCT CCCCTCTCCT CCTCTTCAGC 60
TTCCTCCCTA TTTCTCCTTG CTCCCTAGAG CCATGAGGTT GTCCTCCCTG GGGCTGCCTC 120
AAGATGTTCT CAGAGGCCCC TGGGAGCAGA GGTTCAAGTT CAGCCAAGAA CAGCTATGGG 180
GCAACCAGGG CATTCTGAGA CTGGACTTTA TCCCATGTGG GGTCTCAGCC TTTTGGGTCC 240
CAGGTCCTTT CAGTGGCCCA GAGGAATCAT GAGGCCACTG ACTCCATCTA GGGACCCCTC 300
TGGGCTGCTG TGAGTCCTGG GGCATCCCCT GATTTTGCAG CCTAGGCCCT GTGGCTACAG 360
GGGCAGTGGG GGTACTGCCC TCCAGCAGGA CAGCCAGCAC CAGACCTGGC TGCACCTCCA 420
CCAAACTCCG CGAAAGACCT TGGCCAAGTT GCTTCCCCTG TCTAGAGCTC AAGTGCTCAC 480
TGCGTCATGA TGGCGGGTGG GCTGGAGAAG CCTCCTAAGA ACCTCTTCTA GACGTTGGGA 540
AGATGAAGGA GGGGTTTGGT TAAAGCTAGC AGGAGAATGT GCAAAACTGG GTGGCTCCAA 600
AGTGAGGTCT TTTGCTCAGC AGGAGGGGAC AGCAAGATAT CAAGATGGGC AGATACACTC 660
TGATCAGCAT CTCAGCTGTA CTTGCTGACT CACTCAGCCA GCATCATTGA GTCTCCTCTG 720
TGCCCCGCTG TGGCTGGAGG CCGTGAGGGT GGGCAGTTCT GCAGCAAAGC CACTGAGCTG 780
AGAGTGGTCG GAGGGGAGGA GGGCACGACC ACTTCACATA GGACCTTGCA GGCAGCTGTG 840
AAAAATGTCC ACTGCATATT GTATGTCTAT TGGAGAGTTG CCACGAGTAA TGACATGACC 900
TGCTTTATGT TTTAAATACA GATCACTCCC ATGCTGCATG AAGGGTGGGC TATAGAGGTT 960
AGAGTAGAAC GGAGGGATCA GCTCATGAAT TCAGGATAGT TCCCTGGGCG AAGGCCGCTA 1020
CTCACCATAT AACAGGGAGC ACCAGCATCT CACATTCCCT ACTTCTCTGC CAAACCTGCT 1080
CTGGAATCTC TCCCTTGGAT TCCTTGTTCT GTGGCCTGGT GACTTCACCC TCCTCCCATT 1140
CATCCCGCCA GCTGTCGGTA GTGTGTCAAA AACCTGCTGT GTGCAGACCC AGGCAAAGGC 1200
AAGCACTGGG CTCTCAGGCC CCAAACCCTG CCCTTGTGGC CACAGCTGGT CTCCATTCCA 1260
CCCACTGTTT GCAGATACCC AGAGGATAAC ATGCTCCTAT CTCTGAAATT CCAGGCAGCC 1320
TTGGAGAATT TCAGGGGGAG GAAGTGTCCC ACATTTGCAA ACTTCCCATT ATGGAGCAAG 1380
ACCTTCAAGG AGGCCATAGG GTAAGAAATA AAGGTGCCTT CCTTCCCCTC CTTTTCCTTG 1440
GGCCACTGAA GATAGAAAGT GAGGAAACGT CCCCTTGCCT TGGAGCCCCT ATCTCAGGGT 1500
TCAATGCTCA GCTGACACCA TATAATGAGC TCATCCTGGG TGCTGCTTCT CCCCTCGTGT 1560
ACTCCTGACC ACTTACCACC ATGACTCAAC TTCCAGGGAC CAACAGCAGC TCTGTCCTGC 1620
CTGGTCAGCA AAGCACAAGC CTGAGTTTCC ATTTTCAACA GAGATATAAG TTCATTCCTG 1680
AGTGTGAGTG GCACCTTCAA CGTCTCCTAA GGCCTTGTCA TCTGCACAAG CTCTGGGCGA 1740
GACCAGTTTG GACTCAACCC CAGTGTCATC ATGGGCCCTT GCTTGAGCTT GGGCAGATCT 1800
CAAGGCTGCA TAACCTTTCT GAGCTTCAGT TTCCTCAGCT GGAAAATGGA GAAAACACTG 1860
AGCTCAGGGC CACTGTACAA AACATAAAAT AATGTAAATA AAACACATGA TTCATGGTAG 1920
GTGATCAAAA AATATCACTG CTTGCCCTTA CCTTTTGGTA ATTGATGTGG GTTCTGGACT 1980
TACCATCTTA CATTTCAGAT AGGTTTCCTA CAATTAAATT TTGGAGTGGA TGTATTGTAG 2040
AGGTTAGTTT GAATAATACA CATGCAGTGG TCTCATTCTG ACCATGAGGT GGAATAATTG 2100
GTCCTTACAG AGTGGCCTGA AGTTGTTTTT CCAAACCAGC TCTCTTTGTC ATCTCATCCA 2160
GAGGTCCCTG TGGAGGGACA GCAAAGGAAG CTACCCAGAT TCTCTGGTCC AACTGGATGG 2220
GAAGACACAG ACTAGTGGCA GATGAAGGAC TTACCTATGT TTGTACATTG AAGAGATGCA 2280
GATCTAGGGC TAGAAATCAG GTTTTCTTTC TTTTCTCTTC CTTCCTTCCT TCCTCCCTTC 2340
CTCCCTTCTC CTCTTCCTCT CTTTCTTTCT TTCTTTCTCT CTTTTCTTCC TTTCTGATTG 2400
AGTCCACTCT ATAGCCCAGG CTGGAGTACA GTGGTGTGAT CTTGGCTCAC TGAAACCTCC 2460
GCCTCCTGGG TTCAAGCCAT TCTCCTGCCT CAGCTTCCCA AGTAGCTGGG ATTACAGCTG 2520
CCCGCCACCA TGCCCAGCTA ATTTTTGTAT TTTCAGTAGA AGACGGGATT TCACCATATT 2580
GGCCAGACTG GTCTCGAACT CCTGACCTCA AGTCACCTCT TGCCTTCACC TCCCAAAGTG 2640
CTGGGATTAC AGGTGTGAGC CACTGTGCCC AGCCCAGAAC TCAGGTTTTC TGATTCTTGG 2700
ACAGCTTGGT CTCCTGGGCA GCCTTTATCT GGACTTAGAA GAGCAGAACT GATAGAGGCA 2760
GGTGAAGTGG GGCTGAGCTC CCTAGCCCAG CCTGATTCTC TGTGCCAGAC CACCCAGATG 2820
ATCCCCACAA GAGGAAGCTT GGCCCTGAAG TTCTGGCGGG TGACTTATTT CCTGTCCCCT 2880
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