Tag | Content |
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EnhancerAtlas ID | HS105-48606 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:238577660-238579990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr2:238579015-238579026 | GGCTGTGATTT | - | 6.02 | ZNF263 | MA0528.1 | chr2:238579538-238579559 | TCCTCCTCCCTCTCCTCCTCC | - | 10.7 | ZNF263 | MA0528.1 | chr2:238579535-238579556 | GTCTCCTCCTCCCTCTCCTCC | - | 7.39 | ZNF263 | MA0528.1 | chr2:238579541-238579562 | TCCTCCCTCTCCTCCTCCTCA | - | 8.73 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_00318 | chr2:238578386-238579773 | Adipose_Nuclei | SE_01566 | chr2:238578559-238580557 | Aorta | SE_02327 | chr2:238577505-238579631 | Astrocytes | SE_11030 | chr2:238579689-238588466 | CD20 | SE_25815 | chr2:238577514-238579766 | Duodenum_Smooth_Muscle | SE_26722 | chr2:238578197-238579893 | Esophagus | SE_29646 | chr2:238576186-238581238 | Fetal_Muscle | SE_31908 | chr2:238578660-238579593 | Gastric | SE_36919 | chr2:238576168-238588058 | HSMMtube | SE_40633 | chr2:238577886-238580638 | Left_Ventricle | SE_42111 | chr2:238577997-238580047 | Lung | SE_44590 | chr2:238576694-238580615 | NHDF-Ad | SE_44921 | chr2:238577606-238579710 | NHLF | SE_45786 | chr2:238576920-238579936 | Osteoblasts | SE_48071 | chr2:238577719-238580655 | Psoas_Muscle | SE_48757 | chr2:238578132-238580200 | Right_Atrium | SE_51094 | chr2:238577543-238580570 | Skeletal_Muscle | SE_51777 | chr2:238576746-238580119 | Skeletal_Muscle_Myoblast | SE_52590 | chr2:238578029-238580125 | Small_Intestine | SE_53427 | chr2:238578743-238580684 | Spleen | SE_54582 | chr2:238577649-238580246 | Stomach_Smooth_Muscle | SE_58523 | chr2:238563966-238621920 | Ly1 | SE_59868 | chr2:238570692-238624050 | Ly4 | SE_62022 | chr2:238577134-238613107 | Toledo | SE_63565 | chr2:238576732-238580221 | HSMM | SE_65656 | chr2:238578384-238580104 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 238578400 | 238578874 | chr2 | 238578306 | 238578453 | chr2 | 238578518 | 238578831 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I237667 | chr2 | 238576379 | 238581116 |
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Enhancer Sequence | AAGAAATAAG CGTAACTCTT GTATCAAATG CTCTGTAAAA ATGTTTTAAT GGCCACAAAA 60 TATGGCTTTG AGGATGCACC ATCACGTCCT CACTTCCGTA TTGCTGGACA CTGAGGCTTT 120 TGTGTTTGTT TACTGCGGTG AATAGCATTG CAGTGAACAT CTTTAAGAGT GAGGTTTTTC 180 TACTTCAAAT TATTTCCTTA AATTAGAATA TTAGAAGTGC AATTTAAACC CCAAACCTAC 240 AAACACGGTT AAGGACCTGG AGCTTTGCTT TCCTGAAAGG GTGTATCAGT TTACACTTGC 300 ATTTGTGTTG TCTGAGAGTG TCTTGTTCAT CACAGGATTA AGTACTGTGA TTATCTCAGC 360 TTTGTAAATT TGACAGCTAA AAACTGGCAG CTAACTGATT CTTAGGTATC TCAAGTTCTT 420 TTTCAAATCG TCAAAACGTG TCTTAGAGTG AGTGTTGATA TTTTCTTGCT GATTTGTGGA 480 TTGCTTATTA ACCTTTTTCA TAGTTGTTGC AAATATTTTT TTTCAGTTTA GATTAGGAAC 540 TGAATATCTT CCTCATGTCT TTAAAGAAAT ATGCCTGACC AGGTGCTTGA TAACCCTAAA 600 CGGAGTTTCC TGCCGGGCTT TCTCTTGTAT GATGTTGAGG CCGTCACGGT TTGTTGAGCA 660 GAGGAGTGAG TGCTAAAAGC TGGAGTTCAG CAGAACCACA GTGATGCCTC CACCCCGGGT 720 AAATGCTTAA CCACACTCCT CCCTGTAAAA ATAACGGTGT CATTAAACAT GGACCGGCTG 780 TTCCATGAGC TCATTCCTAG GAAACAGTGG CTGAGTAGCA GAAGCCTGAC CGGTCTCCAT 840 TTCCGCCCAA ATGTGGGATG TGTGCACGTG GCATAGAGCC TCGCACGTTG CTTTTGGGAG 900 AATCAGCTTG AGTCAACTTC TGGCAAAAGA TTGGGGCCGT CTTTGGACAG ATTTGAATAT 960 TAGACACCAT ATCATCTAAT GAAAACCAGC TGGGAAGAGT CAGTTTTCCT GTGTTCTTGG 1020 GCATTTGACA AATGGTGGGA GATAGTTCTA ATTTTAGAAA GGAAAACGTA ATGCATATTC 1080 TCATGATGAT TTGTCAACTG GATATTTTGC AGAGAGGAAA ACGTCTGAAA TGTCCCAAAT 1140 AAAGCTATCT GCTGTCATGA GAACACAGCT GGCAGGGCAG AAAGCAGTGT CGATCAACAG 1200 GAGGTCGTCC TGCACCGGGA CGTCAGTGCC CCGACACCTC GGTGTGTCCC TTGGCTGTGT 1260 GGCCTTGGGC AGGTCACTGG TCAAGCCTGA GATAATGACA TTGGTCTGCT GGGGAGCAGC 1320 GGCCCTAGGC CAGATGTACT AGGAGGCCCC TTCCTGGCTG TGATTTTAAG ATGGAGGGGA 1380 AAATGTTTAT TTGTTCTGTG AAAGCCAGGG GTGGGGTAGG ACAGAGCCAG CAACACCGAC 1440 AGCCCATCAT GCTGAGCCAG AGGTCTGCTG AGCTGAATTG AAGCTGTGTC AACTACAGTA 1500 CGTGCCTCAC CGAGCCTCAG TTTCCACATT GGTGCTGTGC AGATGATAAT ACAGACTTTG 1560 CAAGGCTGTT GAGACTTACC TGCACTAAGA CATAGAAAGT GCCCAACACA GCGCCTGCAG 1620 GGCCAGCACT CGGTGGCAGT CTAAGGAATG TCTGTCACAG CGCTCCCAGA TGGCAGGTCC 1680 TGCCTGCCTG GGCCCAGCTC TGGCTGTGTG GCTCAGGACT ATGGGACCTC TGCAGGCTGC 1740 GTCCCCTGCC TGCCTCAGTT TCTGCGTCTA AGCTAGAAAG CATGATTGTT CCTCCCCGTG 1800 GGGCCGTTAC GAGAAGCAAG CACATGGAAG CGTGCCAGGC ATTTTCCGAA CGTCTGGAAC 1860 ATCCTCAGCG GCAGGGTCTC CTCCTCCCTC TCCTCCTCCT CACTTAGAAA TATTTTCCCT 1920 GGGAGTCCCA CGGAGGTCGT GAAGATGACA GAGGCTGCTG GCACTAACAG CTGTGTGGGG 1980 CAGCCCAAGC CCCTACTTTG AAAGTTCCAT TCCATCCCTC GCATTTCATC TGAAGAGCGC 2040 TATGTTCTCC CTGGGGAGAA CTGGCCTGTT GCATATGAAG AGTCCAGAGA TTTTGAACAA 2100 GGGAACCCCT TCAGCTTCGA ATGACCATTA CCGTTGATGA TCCCAGAAGT TCCCTTTCCA 2160 AGCAGTGACC CATGGACTTG TGTCCCTCGT GTGATAACCT GCACTACACA CATATCCTAC 2220 AAGTGTCCAT AGTGGTTATA AGCTGCCACA GCCATACAGA TCTGAGAGCC AGAGGCCTTC 2280 AAACCAGCTA AGGCTCTGAA ACACTTCAAC TCCACTTAAG AAAACAAATC 2330
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