| Tag | Content |
|---|
EnhancerAtlas ID | HS138-21204 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr2:120994970-120997970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:120996885-120996903 | GGGAGGAGGGCAGGGAGG | + | 6.27 | | KLF13 | MA0657.1 | chr2:120997327-120997345 | TCAGGAGGGGCGTGGCCT | - | 6.02 | | KLF14 | MA0740.1 | chr2:120997330-120997344 | GGAGGGGCGTGGCC | - | 6.25 | | Klf12 | MA0742.1 | chr2:120997329-120997344 | AGGAGGGGCGTGGCC | - | 6.07 | | MYC | MA0147.3 | chr2:120996920-120996932 | AGCCACGTGCTC | + | 6.04 | | NKX2-3 | MA0672.1 | chr2:120997956-120997966 | TTCAAGTGGT | - | 6.02 | | SP1 | MA0079.4 | chr2:120997331-120997346 | GAGGGGCGTGGCCTC | - | 6.5 | | SP3 | MA0746.2 | chr2:120997331-120997344 | GAGGGGCGTGGCC | - | 6.18 | | SP4 | MA0685.1 | chr2:120997329-120997346 | AGGAGGGGCGTGGCCTC | - | 6.53 | | ZNF263 | MA0528.1 | chr2:120996281-120996302 | GGAGGAGGACAGGCTGGGAAG | + | 6.06 | | ZNF263 | MA0528.1 | chr2:120995484-120995505 | CCCTCCCCTCTCCTCTCCTTT | - | 6.33 | | ZNF263 | MA0528.1 | chr2:120996883-120996904 | TGGGGAGGAGGGCAGGGAGGA | + | 6.34 | | ZNF263 | MA0528.1 | chr2:120995462-120995483 | TCCCCTCCCCTCCCCTCCCTT | - | 6.47 | | ZNF263 | MA0528.1 | chr2:120995472-120995493 | TCCCCTCCCTTCCCCTCCCCT | - | 6.9 | | ZNF263 | MA0528.1 | chr2:120995466-120995487 | CTCCCCTCCCCTCCCTTCCCC | - | 7.03 | | ZNF263 | MA0528.1 | chr2:120995479-120995500 | CCTTCCCCTCCCCTCTCCTCT | - | 7.08 | | ZNF263 | MA0528.1 | chr2:120996886-120996907 | GGAGGAGGGCAGGGAGGAGGA | + | 8.95 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27989 | chr2:120995243-120998525 | Fetal_Intestine | | SE_28776 | chr2:120995138-120998740 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 120995093 | 120995456 | | chr2 | 120995613 | 120997953 | | chr2 | 120995461 | 120996023 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I120237 | chr2 | 120994937 | 120998381 |
|
Enhancer Sequence | CTCCAGGTGC ATCTGGCTGC AGCACTCTGG GAGGGGGCCC GAGGTGCATG CAGATCTTGA 60
GTGGGTCTCA GAGAAAGAGA CACACAGGCC CCACATGCGT GTGCACACGC ACACATGGGC 120
ATGAATGTGG GTACGAGGCA TGTGTGCTCC ACACGCTGAC TTCACTGGGA ACACTGACCC 180
CAGCTGCAGA GAGACCGGAG CAAGGGCTGA GGGAGGCAGA GTGAAGGAGC GCTCATCCCT 240
GGGAGGGCGC CTGGGAGGAG AAGTGAGTCA TTGACCAGTG GTCATGGTGA GTTTGCCTTA 300
CGGAGCCATC TCTGGAGCCT GAGGTCACAG GGTCTCTGGA ACTGGCCCTT CAAGTTCCTG 360
GGAAGGGTTT TGACAGGGAA GTCGTCCACA AGGGCTTTCC CCCACTGGAA CACTGCCTAG 420
CCTTCTCAGA AACGCCCCAT GTCTGTGGCA GGCTTGGTGT TCCTCCTGCC ATTCCAGGCT 480
TTCTGCTGCC CCTCCCCTCC CCTCCCCTCC CTTCCCCTCC CCTCTCCTCT CCTTTCCTTT 540
CCTTTTTTTA AATAGAGATG GGGTCTCCTC ATGTTTTCCA AACTGGTCGC AAACTCCTGG 600
GCTCAAGCAG TCCTCCCACC TTGGCCTCCC AAAGTGCTGG GATTACAGGT GTGAGTCACC 660
TTGCCCAGTA ATTTGTGTAA GCATATACCT TGGATTCTCT ACTAAACCGC CTAGTCTTGC 720
CAGTCACTTC CTAGTCTTTC CTGCCTCCTG GCCTTCCTTT ATCTCAGTCC CCTGCTGCCT 780
GGAATGCTCT AATTCTCTCT CTTTCTCTCC CTCTTTTGTG TTTGTCAGAA TCCTCATTGT 840
TTTTTAAGCC CACTCAAGCC TCAAGCTCCA CCTCTCCCAG GAAACATGGG GGCCTACTTT 900
AGTCGAAGAA GACTCTTAGC TCTGAAGTTC TTTGAAATCA TCTCTTCGCC TGAGGCTTCA 960
GTTTCCTTAC CTGTAAAAAT GAGACAATAC CATGTCATGG TTTGTTGTGA ACATTCCCTG 1020
TGATGACCTT CATAACAGTG GCCAGCACGC AGTAGGTTCT CAGTGAAATC CTCATTCCTT 1080
TCCTGCTTTA CGCCAGGCAC AAAAATACAG ATGTGAGGTG CACCCCTGGC TTCTCAGGAG 1140
GGAGCAGGGC TGGGGTGGAG GAGGCCTGGG TGAGGGGTTC CATACCTACC CAGGGAAGGG 1200
AAGGGATGGC AGGAAGCCTT TGAGAAGACC TGCTACTGGG CTGGGTTTGA AGGACAGTTA 1260
GAGGCCATCA GGAGCACCCG AGGAGCAGGA GTACGGTGAG GCAGTGGGGC AGGAGGAGGA 1320
CAGGCTGGGA AGATGGGAGA CAGGTGGTGG GAGGGGCTGG GTGCGGGGCA CTGTCGGGGG 1380
CAGCCGGAGA GAAGACGAGA GCCTGGACTT TATGAAGAGG TGAGGAAGTC ACTGAAGGAG 1440
TTGAGGGCGG AGGCAACAAG TGGGAGAGGC TGAGCCAGGA GAGGCGGCTC AGTGGCCTGC 1500
AAGGGTGGGT GGGGACCAGT GGAAGGCAGC CCTGACTCAG GCTTAGTCAG AGGTCCTGGT 1560
CCAAGGTCCC CTGCCCGCTC CCCGCTCCCC GCTGCAGCCT CACAGTGCCC TTCCTGGAAT 1620
AAAAGGTGGA AAATGAGAGT TTGCTGTTTG GGGCTGCCAT TCAACTTGCC TGGGCAGGGA 1680
GGATGATGGC TGAGGGCCGC CAGCATCCAC GGCCCTGCTC AGTCCCCATC TCCTTGCACC 1740
CACTGTGGTA ACCAAGCTCC CCACCCTGAC ACCTGGCTTG TCTTTTCTGG GGTGGTTTCT 1800
CCCTCAGGGA CTTCGCTCCT CTGTTCAGTC TCCGCCATTT GCACAGCCCC TCAGCTGAGT 1860
CGGTTTCAAG TGAGCAGAGC ACACAGGGGC TTTGAACACC AGCCATGCCG GGCTGGGGAG 1920
GAGGGCAGGG AGGAGGAGTG TGGCAAAGGC AGCCACGTGC TCCACGTGTT CCTCTGGATG 1980
CCCCCGCTCC TCCTGGCGCC CCGTGAGGGT CTGTGTTGGT CCCTGTTGTG CCCTGATCCC 2040
CAGCACCATG CCTGGGGAAC CGTTAAATGA ATGCTTATTG AACGCCAGGG TCACTGTCTC 2100
CAAGTCTCAG GTGTATCGCA GGTGCACAGT ACCTGCCTCC GCCTTGGATG CCTCTACCCC 2160
ACCACAGTAG TATAATTGCC CAGGATGTGG GGCAGGGGCA GAGCGACAAG GGTTGGGGGA 2220
GATGACTCTC TCAGCCCTCC CCTCAGCAAG CCCTCTGCCA GAGTCTCACT CTGTCCTCCT 2280
CCGTGCATTC CGAGAGGTAA GCGCGACTAG GAGTGTGGGC CCAGGTGACC TACGACTGTT 2340
CGCGGGGGAT GGGGCCGTCA GGAGGGGCGT GGCCTCCACT CCATGCCTCT GAAATGTGCT 2400
GGCCTCTGTC TGGAAATTGC TCATTTTTCT TACCACTGAG CTTGGCAGTC ATTGGGGAAT 2460
TTCTGGAGGG AGGGGGGATC CTGGAAGGAA ACTACCGTGG GACCTGTTGT TTCCCCAGAA 2520
GCTCAAACAC AAAGAGAGGA TGGAGTGGAG GTGGTGCTGC AGAGGGGGCT GTTTTTTCCC 2580
TTAAGAACAA GCTGCCTCCT GTCGGAAAAA GGAAGGCCGT TATCCTTTCA TCTCATGTTT 2640
TTTTCCTCCA ACCCCGGGTC TCTGTGTGGG ATTTCAGCAG CGGGAGAGCG GGTGGCAGGA 2700
GGAGGTCTCT GCATGAAACA GCGGCAGTCA GGTGGGTGCC CGCCCTCGGT GTGGATTGCA 2760
CTTCGAAGCC CCACAGTGAC CTTGTGACTT GCCTGTTGTT ATCCTCATTT GCCAAAGGAA 2820
GCTCAGAGAG GTAAACAGAC TTGCCTGGGG TCACACAGCA TGTACTCATG GAGCTGCTAC 2880
TTTTTTATTT TTATTTTTAT TTTTTTTTGA GACAGGGTCT CCCTCTGTCA CCCAGGCTGG 2940
AGTGCAGTGG CGTGATCTTG GTTCACTGCA ACCTCCACCT CCCAGATTCA AGTGGTCCTC 3000
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