| Tag | Content |
|---|
EnhancerAtlas ID | HS138-03233 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:204071510-204074320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr1:204073699-204073713 | ATTCCCCTGGGACT | - | 6.33 | | EBF1 | MA0154.3 | chr1:204073699-204073713 | ATTCCCCTGGGACT | + | 7.17 | | FOSL2 | MA0478.1 | chr1:204073903-204073914 | CTGAGTCACCC | - | 6.02 | | IRF1 | MA0050.2 | chr1:204071935-204071956 | ATAGAGAAACTGAAACTTCCC | - | 6.17 | | IRF9 | MA0653.1 | chr1:204071937-204071952 | AGAGAAACTGAAACT | + | 6.28 | | JUNB | MA0490.1 | chr1:204073903-204073914 | CTGAGTCACCC | - | 6.02 | | KLF4 | MA0039.3 | chr1:204073569-204073580 | GCAGGGTGTGG | - | 6.62 | | ZNF263 | MA0528.1 | chr1:204071742-204071763 | GGAGCAGATGGAGGAGGAAGA | + | 6.48 | | ZNF263 | MA0528.1 | chr1:204071751-204071772 | GGAGGAGGAAGAGGGTGGCGG | + | 6.66 | | ZNF263 | MA0528.1 | chr1:204071748-204071769 | GATGGAGGAGGAAGAGGGTGG | + | 6.71 |
|
| | Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
| SE_01182 | chr1:204071129-204074607 | Adrenal_Gland | | SE_06365 | chr1:204070800-204074466 | Brain_Hippocampus_Middle | | SE_24644 | chr1:204072637-204073956 | Colon_Crypt_2 | | SE_29514 | chr1:204070868-204072610 | Fetal_Intestine_Large | | SE_31799 | chr1:204070890-204072352 | Gastric | | SE_31799 | chr1:204072461-204074581 | Gastric | | SE_34793 | chr1:204069193-204075827 | HeLa | | SE_42361 | chr1:204069421-204075729 | Lung | | SE_47675 | chr1:204073025-204073996 | Pancreas | | SE_49400 | chr1:204070904-204074543 | Right_Atrium | | SE_50648 | chr1:204070818-204074547 | Sigmoid_Colon | | SE_53078 | chr1:204070806-204074527 | Small_Intestine | | SE_54451 | chr1:204071112-204074613 | Spleen | | SE_65332 | chr1:204070923-204074836 | Pancreatic_islets | | SE_68685 | chr1:204070894-204072274 | H9 | | SE_68685 | chr1:204072447-204074590 | H9 |
|
| | 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 |
| GH01I204100 | chr1 | 204069922 | 204075641 |
|
Enhancer Sequence | TGAGGGAGCT CATGAGTTCT GCAGAGCTTT TGTGTCATCA GCCGGGGAAG GGAAGGCACC 60
GTGGCTTGGC CAGATAAGCG GTGGCGCTGC GAATGTGGGG CTTCCTTGGC AGATTTGTAG 120
CCTTTCCGCC TGTTTGCACT GTGGGGCACC TGCTGGGGCT TCCAGGGTGG TTGGGGACAT 180
CAACAGGGCA TTCAGAAAAC TGATAACCTA GGCTAGGGAG GGAGACCTAC ATGGAGCAGA 240
TGGAGGAGGA AGAGGGTGGC GGGCCCTGGT GTTCTGCAGG TGCATGTCTT CTGCTTGTTT 300
GACCATGTGG GGGAAGGGGG TGGCGGTGGG TCAGGGAGCA AACATTTTTT TGATTTTCAC 360
AAACACCATC ATATTCAGTC TTCTCTATCT CTATGGGGTA GGTGTTATTT GTTCCCATTT 420
TAGAGATAGA GAAACTGAAA CTTCCCCATG GCCACACATC TAGTGGTATA TAATAGAGCC 480
AGTCTTCAGA CACAGGTCCA TGTGACAAAG TCCTTTTTCC ATTAGCCACA CCAGGATGCC 540
TCCCAGCAAT GCTGGGTCAT CACACCCACC CACCTGCCTC CGGAAGAGCT GGGCTGGCTG 600
GGGAGGAGAA TAGGGTGTGA GTCCTTCTCC CCCTTGCCCT GGGGGCAGGG AGGGAGAGGG 660
ACTCCTTCCT GCTTTAGGGC TCTTTCTCCT TACCTCCTTC CCTGAACATA TATTCTGTAC 720
CAGATTCTGT AATTATACCT TATCTCTTAC TCACAAAATA GTTCTTGGAA TCTCTATTTT 780
ACACATGAAG AAATGGGGGT TTTGAGAGGT GAAGTCTTTC CCCCAACTTG CCAGAGCTGC 840
CTGGGTTTCT TTTGACTAAG TTTTCCTTGG CTATGACTCA AGTCAGAAAC AACTGCAATC 900
CTGTAAGAGG TGAAGACAGT GGCCATTCTA TCTCTGCTGG ACCAGAGCCT GTTATTTTGC 960
ACCGAGGAGA GTGGCCAGGG CATCAGCTGA TAAATGAAAG GATGTGGATT TAGACATCAG 1020
CGAGGCCTGA GTTCAAATGC TACTTCTGCT GGGCCCTCAG TAGGACGTTC TAGCCCCCGA 1080
GCCTTAGTCT TTGTAGTGTT CTTGTGAGGA TTAAGCAGGA ATGTGAATGA AGAGCCTTTC 1140
ACTTAGTGCT TGCAGCCAAG TAAGTGCTGT AGCATTGCAT GCTTGCTTTT TGCCTCCCAT 1200
TCCTTTGGTC AGTATTCAGG GCTATCCCCC AAGGGGCCTT TGACATGGCC AGTCAGCCTC 1260
AGCTGCACAA TTTCTGCATC TCCCAGCCCT AGGCTGGGCA CTGTCCCTGC AGGAAGCCAG 1320
ATGTGCTCAC CTGTCCAGGA CACAGGCTTG GCCTTGCCAT TGGGAAACAA GGATGAGGCC 1380
TACCCCTGCC TTCTAGCACT GTTGGGGTGC AGGAGAACCT GGAGACAGGC TTGGGTTCTA 1440
GAGGCAGGAA GGCCTCCAGA GAAGGGCCTC CTAGAGACAC TGTTGACCTC TTCTCGGTTT 1500
GGGACCTTCT GGAGGCACAC ATCACACTGG GAGCCTCAAT GGCGCTTTCA AGCAGTCCCA 1560
TCTGTCTCTT TCTCGACCCA CTCACTGGGT TGGGAGAAGA CTCAGGTGCC TCTGAGGCCT 1620
GAGGACCAGG TGGGAACATC ACAGCTACAG TCTCTCCCTG GCCACTGTTT TCCTTTGTGC 1680
CCTTGGGCCA GGGTCAGCTG AGTCCCGGCA GCCACAGAAG CTCAGGCTGG ACTGTGATTC 1740
TGTACCTGAG GTGCTGTGGG GAAGTGCCTC TTCTCCCATG CTTGGGAGTT GACCCAGCCT 1800
CTGTCTGATG TTGGCCACTC TACCAGGTGA ATGCCACCCT GACCAGCCTG GAAACAGCCG 1860
AGGGAGTGTT GGCTGTGGCC CCCCTGAGCT GGGCTAGACC AGACCGGCCG TGCCCTGGAT 1920
CTGATACCCC CCAGGGCTCA CAGAGGCTGG AAAGGGTGAG AGGGACTCGC AGGAAAGCTT 1980
TGTCCCAAGC CTGCAGCCAG TCCAGCTCCC AGCTCTGAGT AAACATTAGA GATAGGATCG 2040
GGTGTAGCCA GGAAGGGTGG CAGGGTGTGG TCTGTGAGAA GAATGGCAGG ATGTGGCACC 2100
GGGGCACTGT TCTGGGCACC CACGCCTTGG CCTATTGTTT AGGGCAGCCT GAGGTTCTCA 2160
GCTCTCTGGG GGCTTTCAGA GGAAGTGGCA TTCCCCTGGG ACTCAAGCCC TGCCCCACCC 2220
CTGCTGCATG GATCTCTTTC CCTGGTGATG CCCCTTGGCA CCACCCACTC AGAGCAAGCT 2280
TGGGAGTGGG AGCCAGCAGT GGAGGGGGAT TAGTGTGTGC CCAGCGGGGA AGTGTAGCCA 2340
TTGGCCCTCT CAGAGGGTCT GCCTGTCTGT TCAGGCTTCC TGTACCCCAG GGTCTGAGTC 2400
ACCCGTCATG CTACGATGAC TGGAATTTAT CTCTATCTTT ATCTTCATCT AGATATTTTT 2460
TGTAGGGTGG GGGAAGGCTG TCGTTGTGGA GGGAGGAAGG ACTGACAGTA AAAACTCCTT 2520
TGATTCCAAT CCAACAGGGT CAGTTGTTGA CTGGTTAGAA GAGGAAGTGG CTGGTGATTT 2580
GTTTTGGGCA GAAAGGGGCT AGGTTTGTGT GCGCCTGTGG GTTGGTGGGG TTCAGAGGGG 2640
CCGTGACAGG GCTGGTTGTG GGGAGGAGAG AGGAAGAGGA TCGGCACCTG CAGCGGGCTT 2700
TGTCATATAA GCGCCATGCT TTGAGCCACT GTCCCTCCAT GGAGGCGGGT GCCTCTCTAT 2760
ACCTTGTCTC AGGTGCTGGA TTTGGGGGCC TCGGGGCCTG GTAGGCACAA 2810
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