| Tag | Content |
|---|
EnhancerAtlas ID | HS153-02568 |
Organism | Homo sapiens |
Tissue/cell | Osteobl |
Coordinate | chr2:28581200-28584530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr2:28582101-28582118 | CAGGTCACTGTGAGCCT | - | 6.29 | | Foxd3 | MA0041.1 | chr2:28581551-28581563 | AAACAAACATTC | - | 7.22 | | JUN | MA0488.1 | chr2:28582256-28582269 | AAAATGACGTCAT | + | 6 | | JUND(var.2) | MA0492.1 | chr2:28582255-28582270 | GAAAATGACGTCATG | + | 6.4 | | MAFF | MA0495.3 | chr2:28583982-28583997 | GGGCTGACTCAGCAC | - | 6.05 | | MAFF | MA0495.3 | chr2:28583982-28583997 | GGGCTGACTCAGCAC | + | 6.08 | | STAT1 | MA0137.3 | chr2:28581543-28581554 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr2:28581543-28581554 | TTTCTGGGAAA | + | 6.32 |
|
| | Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
| SE_20015 | chr2:28580994-28584412 | CD56 | | SE_22508 | chr2:28581176-28584226 | CD8_primiary | | SE_23078 | chr2:28581214-28583029 | Colon_Crypt_1 | | SE_23736 | chr2:28581652-28583544 | Colon_Crypt_2 | | SE_24706 | chr2:28581304-28583615 | Colon_Crypt_3 | | SE_27327 | chr2:28581171-28583319 | Esophagus | | SE_27724 | chr2:28581678-28582847 | Fetal_Intestine | | SE_28654 | chr2:28581848-28582655 | Fetal_Intestine_Large | | SE_31386 | chr2:28581241-28583563 | Gastric | | SE_34659 | chr2:28581009-28584958 | HeLa | | SE_50076 | chr2:28581169-28583418 | Sigmoid_Colon | | SE_51112 | chr2:28583810-28584935 | Skeletal_Muscle | | SE_52349 | chr2:28581244-28583067 | Small_Intestine | | SE_53354 | chr2:28581643-28583407 | Spleen | | SE_62927 | chr2:28581266-28660518 | Tonsil | | SE_65553 | chr2:28582948-28584730 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 28583371 | 28583537 | | chr2 | 28583784 | 28584228 | | chr2 | 28581286 | 28582890 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I028358 | chr2 | 28581236 | 28585206 |
|
Enhancer Sequence | GCAGAGGGAG CCTGCTGGGC ATGGGTAGAG AGCCCATGAG AACCTGGTGC AGGTGGAAGG 60
AAAGGGGACC CCACAGGGAA GGTAGAAGGG CCAGGGCTTT CCCCAGCAGT GGCCAGATCT 120
GAACAGAGAT GACTCTGTGT TGCTGTGGCC ACTCCAGACC CCAGACCGCA GCCTGATATC 180
CAAGCTCCCG AGGGAGCAGA ATGCATCAGC CACCTCAGAG AGGAGGCGCA GCCCAGTCAG 240
GGCCCCACGT TGTCACGGCT CCAGCTGTCC TCAGGAGGGA AACTGTCTTG CAAGCCTGGA 300
GACTTCTGGT TGCTTCTCGG AGGAAAGGTA GCATCTCCCT TCCTTTCTGG GAAACAAACA 360
TTCCCGAGTA CCAACTGCGT GCCAGGCCCA TTGCTAGCTG CAATCTTAGG CGAGTCCCAA 420
ACCTCTCTGA GACTTGGGCC TGTCATCTGG AAACAGAGTA GTCTATAAAA GATTGACTTC 480
AAAGGGCTGT GAGGACAGTC AAAGAGACCA TAAAGCACAG AGCTTGGGCA GGGGTGGGCA 540
TTCAGGAGAG GTGGTGGCCC CTTCCCCTGT GCCTGCCCCT GGGAAACCCT GTCCCCTACC 600
TGGCTGGCAG CACAGGAGAC GTGGAGAAGG GACAACCCGG TCTGGGGACG GGGCGGTTTC 660
TCCAGGCTGG GCTGCCACTG TCTTCCTTCC CTGTGTGGGT GGTGGCTCAG GGCCTGGTGG 720
TCTGCCACAA AGGTCCAGAA GGTCCACCCT TTCTGGTGGC TGGGGGTGGC AGTCAGGGGC 780
TTCAGGACAA GCCTCTGGCT GCTGTGGCCC CCTACCCTTC CTCTGCACCT TGGGAGCCCC 840
AGCCCCTGGG CTGTCTGAGT CTATGCTAAC AAAGTAGGAG CCAGAAACGT TCCTTTAGAC 900
ACAGGTCACT GTGAGCCTTG GCTAAGCCTG GGGACCTCTT CTCGGCCCTG GCTACGGCCC 960
AGATGCCCAC CCTGAACCTT CCACGAGTCA GGGCAGGCAC CATTTCCCCA GGACCAGCTG 1020
AGCAGTAAAG TCTCTTCTGG TTTATCTGGA GGAAGGAAAA TGACGTCATG AGGTAAACCG 1080
CACAGCCTGA AACCACGAGG CTGGGCGCCC CAGTGATGTT TGCTTTTCAG CAAAAGTCAC 1140
CATGCACACA GAGGGACAGG GAGCCCAGGC CATTGTGGTC AGAGGGTCAG GGGGAAGACA 1200
GAGGGAGATT TTTTAACACG GAACCACAAG GAAGGAGAGG CCCCCGGAGA GGACGGACGT 1260
CAGAGGCCAG AGGGCGGCTT CCTGGGGTGC TGTGAGAGAC TTGTCACCTG CTGGGTGGGG 1320
CAGTCTCTGC TGGTGTCTCA CGAGGTCTCG GGCTTGGCAC CTGAGGCATG CAAAGTCACG 1380
TTTGCCATGG CGGGCACAAT AATAGTGGCA AGAATAATAA TATCGATAAC GCATCCTGAC 1440
CATGTGTCTC TGTAGCCCTG TCACCTCCTC ACCACCGTCC CATAAGACGG GACCCTGCGA 1500
GGCAGACGCA GCCTGCACAC AGAGGAGGGA GGGGAGGCTG CTGGGGCTCC GGCCTGTGCT 1560
TTCGCCTCCA GACCATGGAG CTTCTTCACC CACATGCTGG GTGCCGTCCA GCCTGAGGCC 1620
TGTGTGCAGG GTCCCGGTTT CAAGCCCCGA TTCCCACCTG CTAACTGTGA CCCAGGAAGC 1680
CCCACCCCCC GCAGCCCTCA GTTTCTTCAC CTGCCAAACT CCCTGCCTTC GAGGTGAGAG 1740
ATTACGTAAG TAAGGTAAAG CTTATTCTTC GATACCGTTC TCTTACTCTG TCAATGCTTT 1800
GAGCAGGGTT CCCTGGAGAA ACTGGCCCCA AAGCGTGGGC CCAGACACTG GTCTTGATGG 1860
GCTGGCTGAG GCGGGAGCTC CGTCTCATGG GAGTGGATGG GAGTGGCAGG CAGGTGGGTG 1920
GCACCTTCTG TGGAGCGGGG GCCAGTCGGC AGCTTAAACG AGGGCAGAGA GAGCTGTCTA 1980
GGGAGGTCCA ATGGGGCTTC ACTTTTCTCA GGAATCTCAG GGTCTCCAAG CCCCCACTCT 2040
AGGGTGGCAT GAGTTTGGGG GGTTCCTAAA GGAAGTCCCC TGTGTCTGGG TGTGCCTGGG 2100
TGGCAGTGTA GGGGCAGGTG TGGTGCCCAC ATTGTCCATA TGTCCTCACC CGCCCCAGGC 2160
CCCAGGCCCT CTGCCTCAGG GTGGGGCCGC AGCTCAGCTT TGATGCCCCT GAGGGCCTGC 2220
CTGCCGGAAC TGCTGTTTCA GGCAGGAGGT GGGAGGACGC AATGCAGGCG GGGTTGCCCA 2280
ACCAAAACAC CCTCAGCCCA ATTCCTCCCA CAGGCCTCCT GGAACCCGCA TTTCTTCAGT 2340
GGAGTCACAG CTTTTTGGGC TATGGCTCCT CTTTTCAGTT CTTTTTCTTT ATAACACAAA 2400
GACACCATGA GAGAGGCCGT ACTTCACAAT CCCCAAGTGT TAGAAGGCAG AGGGTCTTCC 2460
AGACAGCCAC CACCAGGCCT GTGCTTTACA GAGGAGGAAG CTGAAAGGAC TGGTCCAAGA 2520
CCACACAGCG GGGAGCAGGT GGCAGCACGG ACGCTCGAAG CTTGGTCTCT CGCTGTGGAG 2580
TTTTCTCTCG CCTGTCTCTA CCGCTATCAT CCTAATACTG AAGCATCAGG TCCTTTTTCA 2640
AGACACCACC AGCTACAAGC AGAGGGCAAG CCTGGGGCTG AGAAGCACTG TGGGGAGGAG 2700
GGGTGGAGCT GGGAGAGGGT CACGGGAGTC AGGGGCCAGG GAAAGCTGCC AAGCAGAGAC 2760
AGCCTCTCCT GCCCCTTTCC CAGGGCTGAC TCAGCACCTT ACGCGTGAGG ATTTGTCATC 2820
AACAACTGAC CCCAAAAGCC ATGGTGCCCT GGGGTTGGTG TCCCAGTGAT GCTTTTCTGA 2880
CTCGTGGCCC AGGATGACAC AAAGCCCCAA GGGACAAGCC AGAGATCCCA CTGGCCCAGC 2940
CAGATGCTCC AAGATTCCTT TTGCCTGTAA CCCAGAACTG GCCCACCCTC TTGCCTGGTT 3000
ACTGGGGCTT TCACGAAAGA GCAATGGACA GTGGGAAGGG CTCGCTGTGA GGCAGGATCA 3060
GTCCTGGGGC CCTGGGAGTG TCTCTTCCCT TCCCCGAGCC TCAGTGTTCT TGTCTGTACA 3120
ATGGAAGTTC AGGTCAGATG GTCTCTGGAT TCCTTCCCAG CTCTGAGAAC CAGGTTCTAC 3180
CTCAGCTGTT CTCAGAAAGG ACAGGGTGGT CCGGGCTGGG CATGGGCTTG AGGCTTGTGC 3240
CCCTCTCCTA GCCCCAAGGA CTTCCCATCC TTTCAGGTCC CGCTGGGGCT CAGCTGCCCA 3300
ACTCTGATCA GAAAGAAGAG CTGTAAGTCT 3330
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