Tag | Content |
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EnhancerAtlas ID | HS098-33755 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:238577480-238580150 |
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 | TAATAAGGAA AATTCAGGCA ATAGTAGAAA ATAAAAATTA TGCCTCATAC TTGACCAAGC 60 ACAATACCTG TTAACATTTT GTTTATTTTT CTCCATTCTT TTATCTGTGA CTTTTTTTTA 120 ACATAGTCTC AATTATGTGT CTCTAAATAG CGCATTTTTA AAATCTCCTT TTTTTAAGGA 180 AAGAAATAAG CGTAACTCTT GTATCAAATG CTCTGTAAAA ATGTTTTAAT GGCCACAAAA 240 TATGGCTTTG AGGATGCACC ATCACGTCCT CACTTCCGTA TTGCTGGACA CTGAGGCTTT 300 TGTGTTTGTT TACTGCGGTG AATAGCATTG CAGTGAACAT CTTTAAGAGT GAGGTTTTTC 360 TACTTCAAAT TATTTCCTTA AATTAGAATA TTAGAAGTGC AATTTAAACC CCAAACCTAC 420 AAACACGGTT AAGGACCTGG AGCTTTGCTT TCCTGAAAGG GTGTATCAGT TTACACTTGC 480 ATTTGTGTTG TCTGAGAGTG TCTTGTTCAT CACAGGATTA AGTACTGTGA TTATCTCAGC 540 TTTGTAAATT TGACAGCTAA AAACTGGCAG CTAACTGATT CTTAGGTATC TCAAGTTCTT 600 TTTCAAATCG TCAAAACGTG TCTTAGAGTG AGTGTTGATA TTTTCTTGCT GATTTGTGGA 660 TTGCTTATTA ACCTTTTTCA TAGTTGTTGC AAATATTTTT TTTCAGTTTA GATTAGGAAC 720 TGAATATCTT CCTCATGTCT TTAAAGAAAT ATGCCTGACC AGGTGCTTGA TAACCCTAAA 780 CGGAGTTTCC TGCCGGGCTT TCTCTTGTAT GATGTTGAGG CCGTCACGGT TTGTTGAGCA 840 GAGGAGTGAG TGCTAAAAGC TGGAGTTCAG CAGAACCACA GTGATGCCTC CACCCCGGGT 900 AAATGCTTAA CCACACTCCT CCCTGTAAAA ATAACGGTGT CATTAAACAT GGACCGGCTG 960 TTCCATGAGC TCATTCCTAG GAAACAGTGG CTGAGTAGCA GAAGCCTGAC CGGTCTCCAT 1020 TTCCGCCCAA ATGTGGGATG TGTGCACGTG GCATAGAGCC TCGCACGTTG CTTTTGGGAG 1080 AATCAGCTTG AGTCAACTTC TGGCAAAAGA TTGGGGCCGT CTTTGGACAG ATTTGAATAT 1140 TAGACACCAT ATCATCTAAT GAAAACCAGC TGGGAAGAGT CAGTTTTCCT GTGTTCTTGG 1200 GCATTTGACA AATGGTGGGA GATAGTTCTA ATTTTAGAAA GGAAAACGTA ATGCATATTC 1260 TCATGATGAT TTGTCAACTG GATATTTTGC AGAGAGGAAA ACGTCTGAAA TGTCCCAAAT 1320 AAAGCTATCT GCTGTCATGA GAACACAGCT GGCAGGGCAG AAAGCAGTGT CGATCAACAG 1380 GAGGTCGTCC TGCACCGGGA CGTCAGTGCC CCGACACCTC GGTGTGTCCC TTGGCTGTGT 1440 GGCCTTGGGC AGGTCACTGG TCAAGCCTGA GATAATGACA TTGGTCTGCT GGGGAGCAGC 1500 GGCCCTAGGC CAGATGTACT AGGAGGCCCC TTCCTGGCTG TGATTTTAAG ATGGAGGGGA 1560 AAATGTTTAT TTGTTCTGTG AAAGCCAGGG GTGGGGTAGG ACAGAGCCAG CAACACCGAC 1620 AGCCCATCAT GCTGAGCCAG AGGTCTGCTG AGCTGAATTG AAGCTGTGTC AACTACAGTA 1680 CGTGCCTCAC CGAGCCTCAG TTTCCACATT GGTGCTGTGC AGATGATAAT ACAGACTTTG 1740 CAAGGCTGTT GAGACTTACC TGCACTAAGA CATAGAAAGT GCCCAACACA GCGCCTGCAG 1800 GGCCAGCACT CGGTGGCAGT CTAAGGAATG TCTGTCACAG CGCTCCCAGA TGGCAGGTCC 1860 TGCCTGCCTG GGCCCAGCTC TGGCTGTGTG GCTCAGGACT ATGGGACCTC TGCAGGCTGC 1920 GTCCCCTGCC TGCCTCAGTT TCTGCGTCTA AGCTAGAAAG CATGATTGTT CCTCCCCGTG 1980 GGGCCGTTAC GAGAAGCAAG CACATGGAAG CGTGCCAGGC ATTTTCCGAA CGTCTGGAAC 2040 ATCCTCAGCG GCAGGGTCTC CTCCTCCCTC TCCTCCTCCT CACTTAGAAA TATTTTCCCT 2100 GGGAGTCCCA CGGAGGTCGT GAAGATGACA GAGGCTGCTG GCACTAACAG CTGTGTGGGG 2160 CAGCCCAAGC CCCTACTTTG AAAGTTCCAT TCCATCCCTC GCATTTCATC TGAAGAGCGC 2220 TATGTTCTCC CTGGGGAGAA CTGGCCTGTT GCATATGAAG AGTCCAGAGA TTTTGAACAA 2280 GGGAACCCCT TCAGCTTCGA ATGACCATTA CCGTTGATGA TCCCAGAAGT TCCCTTTCCA 2340 AGCAGTGACC CATGGACTTG TGTCCCTCGT GTGATAACCT GCACTACACA CATATCCTAC 2400 AAGTGTCCAT AGTGGTTATA AGCTGCCACA GCCATACAGA TCTGAGAGCC AGAGGCCTTC 2460 AAACCAGCTA AGGCTCTGAA ACACTTCAAC TCCACTTAAG AAAACAAATC GGAGCACATC 2520 CGTGATCCCA CAAATGCTAA TTTGCTTGTC ACACATCAGA AACCCAGGAA GGCACAGAAT 2580 AGATGCTCTC TTACTGGCTT ATAGGTTGGG TACTTTAAAG TTGGAGACGT TTAAATCAGA 2640 GATAAACCTA TTGTAACAAT ACATTTCATG 2670
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