| Tag | Content |
|---|
EnhancerAtlas ID | HS138-03263 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:205262290-205265720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:205263880-205263891 | GGATGACTCAT | + | 6.62 | | IRF2 | MA0051.1 | chr1:205263976-205263994 | GGAAAGAGAAAGGAAAAG | + | 6.03 | | JUN(var.2) | MA0489.1 | chr1:205263882-205263896 | ATGACTCATCCCCC | - | 6.22 | | JUNB | MA0490.1 | chr1:205263880-205263891 | GGATGACTCAT | + | 6.62 | | PRDM1 | MA0508.2 | chr1:205262631-205262641 | GTGAAAGTGA | - | 6.02 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_02431 | chr1:205262567-205264599 | Astrocytes | | SE_05801 | chr1:205262462-205264469 | Brain_Hippocampus_Middle | | SE_11085 | chr1:205262547-205264187 | CD20 | | SE_26974 | chr1:205262635-205264492 | Esophagus | | SE_26974 | chr1:205265274-205265884 | Esophagus | | SE_29391 | chr1:205262567-205264765 | Fetal_Intestine_Large | | SE_32765 | chr1:205262511-205264574 | H1 | | SE_38936 | chr1:205262243-205265794 | IMR90 | | SE_46173 | chr1:205262329-205265260 | Osteoblasts | | SE_50327 | chr1:205262518-205264578 | Sigmoid_Colon | | SE_52983 | chr1:205262582-205264598 | Small_Intestine | | SE_54130 | chr1:205262477-205264677 | Spleen | | SE_55645 | chr1:205263252-205263684 | Thymus | | SE_56704 | chr1:205262588-205264656 | u87 | | SE_56704 | chr1:205264714-205265918 | u87 | | SE_58462 | chr1:205242169-205295027 | Ly1 | | SE_58967 | chr1:205242236-205295022 | Ly3 | | SE_60263 | chr1:205242326-205284722 | Ly4 | | SE_60576 | chr1:205242267-205294889 | DHL6 | | SE_61365 | chr1:205242037-205294994 | HBL1 | | SE_61423 | chr1:205183427-205322469 | Toledo | | SE_62465 | chr1:205242393-205294944 | Tonsil | | SE_65493 | chr1:205262566-205265065 | Pancreatic_islets | | SE_68815 | chr1:205262515-205265189 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 205262860 | 205263030 | | chr1 | 205265393 | 205265497 | | chr1 | 205262798 | 205264485 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I205293 | chr1 | 205262232 | 205274585 |
|
Enhancer Sequence | GTAGGTGTTA GTTTATGGCC CCAACTTTAT TATAAGTAAA TTCCTTGAAG GAGGGGACGT 60
GCCTCAATTG CTTCTGTATT TTCCATGGCA CCTAGAACAA TAGTAAGGTC TTAATAAATG 120
TTGATGTGTT TATTAGGGAA TGGGTTTTCA CTTGATTTAA CTATCAAGTT CCCCTTTATA 180
AGGGGCTGGG GCCAGGAAAG CGGGTGGAGG CCCTTTATTA AACATTTATT GAGTACCTGT 240
TCTCACTCCT TAGGTTTTCT CCAGTGATGT ATTGCTTAAA AAGCATGTTC ATGTGTTGTC 300
TCATTTAATC CTTGCAGTAA TGTGATGGGT GTGAGCTGAC TGTGAAAGTG ACTCTCTAAG 360
TCATTGCAAT GCACTCTGTG GGAAGAATGT GCTAGCCCAG CAAGGCTGTC TTTGTGATGT 420
CCGATGTGTA CGTGCGTGGG GAGGCGCTCC CAAAAGCTGC GCTGGGGCAG GGTGTCCTGA 480
ACGGCGTTAC CAGATGTATC TTGACAAAGA GGTTGGCACC ACCATGAAGA CCAATTCAAC 540
CAGCTCTCCT AGCCCAGCTT CCATGCTCTT CAAGGAGACT TCCCACTGAA CTTCCGAATA 600
CCCTTGTGTG AAACTGCCAC AGGCAGTGAA TGTGCTCATC AGCAAACCCA AGTATCTGGT 660
TGGTTTGACA GGGGTTTTGT TATTCATTAG AAATGAATGA ATTGGCATGT TGGCTGAATC 720
CATTCCTCTC CTAGAGCTCA GTGAGTCTGC TCCTGAGCCT CCTAGCCTGT TGATAAGCAA 780
GGTTTCTGAG CAGCAAAGTG AGGCTGCTCA CTTTGGCAAA CAGGTCTTCA GGTGAGCCCG 840
GCCACCATGT GAGGCCCTGT TGGCAGGCCA GGCTCTCCCC AGGCCCCACC TGGCCTCACC 900
AATGGCTCTT GGATTCACAG AGGACTGCAC ATTGGACTGG GAGACAGGGC AAGCCAGGGG 960
TCCCTTAGCA GAGAAGGGAT CCCTGCCAGT AACTAGCCTG CTGTGAGTAT GAAGTTGCCA 1020
CTTACCAAGG ACCCTCCTGA TGGACACAAC AAAGGCGATG GGTGATTGCT GCCAGGGCTC 1080
ATAAAGAGGT GATTCAGAAT CTAGCTGGGG GAACTTTGAA AGGTCATTGC ACCTTGACCC 1140
TAGCTTCCAG GCGGGACATG TGGTGAGTTC TGCTGCAATG GCTGGGTGCC CTCACAGGCC 1200
AGAGCTCAGG TTAATGCAGC TCAGAGCTCG AATTCTGATC ACAGGAAGAG AATGGTGAGG 1260
AGGATGGAGG CAGGGGTGCT GGCTGGGCCC AGAACACCAA AGGCAGAGCT GAACACTTCC 1320
ACTGGGAAGT GGGGGTTTTG GCCTCTTGGG CTGGGAAATT CCTGGCCGGC ACTGTCTGTT 1380
TATCAGGGAA GCTGAGTCAG ACTGAAACGT ATCTCCTAAA AAGCTCTGCT ATTTCTAGGA 1440
TTCCATCCGG TCAAAGCCAG CCTCCTCTTC CCTGGGGAAT TCCTTTGAGG GTGGAGAGAT 1500
AGAGGGGACA GACTGGCCTT TTCCTAGACA TGGAAACCTG AAATCTGAGT TTTTGCCCAT 1560
TTATGGACCT GAAATCCCCT CCCCCACCTA GGATGACTCA TCCCCCAGCT TGACCCAACT 1620
GCCCCTAGAG AGGGGAAAGG GTGAAACTGA GATGGTGGGA TTAGCTCAGG GAGGGGGTTG 1680
GAGGCTGGAA AGAGAAAGGA AAAGACAACT GAAAAGGATG GGGAATTCCT TTGCAAAGAG 1740
ATGGTGAGGA GAGGATTTCA GAGCCAAAAA GAGGCAGAAT GAGAAAGAGA GAAAGATTTT 1800
CATCCCAGAG GGAAGCTGCA TGCCTGGCAG AGTAAAAATC TTCCAGGTTA AGGTAGGTTC 1860
AGGCCCTCAC CTTGAGTAAA TTCTGGAACT TTAGTGTGAT CAGAGCCACT TGCCGTGCTT 1920
GTGAAAATGC AGAGATTCCC GTGCCCTCCC TGGGCTGTGA TCCGCTTCCA GGCTCCTTCA 1980
GGGATCTGAA GTAGGAAGTT CTGAAACACA GAAAGAGGAT TGACTGGGAA TCCTTCTCCC 2040
AACCTGGGGC CTCTGCTGTA TAAAGCGACT CACAACCCCT CTGCAGGTGC CAATGTCAGA 2100
GGCAGAGCCC TGGTCCAAGG GTGACGTTTC TAACATTCTT ATAAAAATCT GTGAAAGACT 2160
TTGGCCAGGC CCAGTGGCTC AAGCCTGTGA TCCCAGCACT TTAGGAGGCT GAGGCAGGTG 2220
GATCTCTTGA GGTGAGGAGT TCGAGACCAG CCTGGCCAAC ATGGCAAAAC CCGTCTCTAC 2280
TAAAAATACA AAAAAATTAG CTGGGTGTGG TGGCATGCAC CTGTAGTCCC AGCTACTGGA 2340
GGAGCAGGGG GGCGCTGAGG TGGAGGATCG CTTGTGCTCA GGAGGTCGAG GCTGCAGTAA 2400
GCTGAGATTG CACCATTGTA CTCCAGCCTG GGCCACAGAG TGAGATCCTG TGTCAAAAAA 2460
AAAAAAGACT TTTTATCGGA TGGAGAAAGC CAGTCCCCAC CAGGCCAAAT ATGCCTCCTC 2520
ATTGCAGCAC TGCCCACCTC CCCACATAAT CATATCAGAG AAGCTTTGGA AAGAACTGCT 2580
TTCCTAGTCA ATACAATCCT AGGATCTTTA CAGCCAGAAG GGACTTCTTC AGGTATCATC 2640
TGGCGGGATT TTTCACCTGA AGCAGAAATT CCTTCTAGCA ACAACCCCCA CATCTCTATC 2700
TCCAACCCAA ATCTCTCAAA CTCCAGGCTC CTCATACCAC TTATCTTTGC CTGGAGGCCT 2760
AAGTGCCTCT GACTTCACCT CACACCTCCT CCATCTGCAA GTCTTCCCCG ACCCAGCTAA 2820
TGGACACTCT ACCCTCCAAG TTTCTCAGGC CAGAGACCAT GGAGTGATTC TTGGTTTCTC 2880
TCTTTCTTTC ATACCCTACA TCTAATCCAT CAGGAAAGCC TGTTGGCTCT AGCTTCAGAA 2940
TATGTCAGAA ATCTGACAAC TTGTCATTTC TTTACTACTG ACTCCAGTCC AAGCCCCATT 3000
ACCTCTTTCC AGAATTGGAC AATGTCGACC CTCCCATGGC TAGTCTCAAC AAGCAGAAGA 3060
ATTTTTTTTA ATTCTATCTC AAAAAAAAAA AATGTCATTC CTTTGCTCAG AACTTCCTGG 3120
TGGTTGGCAA TTTCATTCTG AATAAAAGCC ACAGCCCATG TAATGGTTCA CAAGGCCCTG 3180
TGTAATCTAC CTTCCCCACC CTTGTTACCT CTCCTGACAC GTCTTCTGCT ACTCTCTCAT 3240
GCACTCTGCT CCAGCATCAA TGGCTGTTCT AGAACTTGCA ACCTGCTCTT GCCTTGAGGC 3300
CTTTGCAATG GTTGTTCCCT CCACCCTGAA CACTGTTCCC CCAGATAGCC ACATAGCTAG 3360
CTCCACCCCC AACCCCTGCC ACCAGGTTTT TATTCAAATG CCACCTTCTC AGGAAGGCCT 3420
TCTCTGATCA 3430
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