Tag | Content |
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EnhancerAtlas ID | HS094-23632 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr2:238577500-238580260 |
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 | ATAGTAGAAA ATAAAAATTA TGCCTCATAC TTGACCAAGC ACAATACCTG TTAACATTTT 60 GTTTATTTTT CTCCATTCTT TTATCTGTGA CTTTTTTTTA ACATAGTCTC AATTATGTGT 120 CTCTAAATAG CGCATTTTTA AAATCTCCTT TTTTTAAGGA AAGAAATAAG CGTAACTCTT 180 GTATCAAATG CTCTGTAAAA ATGTTTTAAT GGCCACAAAA TATGGCTTTG AGGATGCACC 240 ATCACGTCCT CACTTCCGTA TTGCTGGACA CTGAGGCTTT TGTGTTTGTT TACTGCGGTG 300 AATAGCATTG CAGTGAACAT CTTTAAGAGT GAGGTTTTTC TACTTCAAAT TATTTCCTTA 360 AATTAGAATA TTAGAAGTGC AATTTAAACC CCAAACCTAC AAACACGGTT AAGGACCTGG 420 AGCTTTGCTT TCCTGAAAGG GTGTATCAGT TTACACTTGC ATTTGTGTTG TCTGAGAGTG 480 TCTTGTTCAT CACAGGATTA AGTACTGTGA TTATCTCAGC TTTGTAAATT TGACAGCTAA 540 AAACTGGCAG CTAACTGATT CTTAGGTATC TCAAGTTCTT TTTCAAATCG TCAAAACGTG 600 TCTTAGAGTG AGTGTTGATA TTTTCTTGCT GATTTGTGGA TTGCTTATTA ACCTTTTTCA 660 TAGTTGTTGC AAATATTTTT TTTCAGTTTA GATTAGGAAC TGAATATCTT CCTCATGTCT 720 TTAAAGAAAT ATGCCTGACC AGGTGCTTGA TAACCCTAAA CGGAGTTTCC TGCCGGGCTT 780 TCTCTTGTAT GATGTTGAGG CCGTCACGGT TTGTTGAGCA GAGGAGTGAG TGCTAAAAGC 840 TGGAGTTCAG CAGAACCACA GTGATGCCTC CACCCCGGGT AAATGCTTAA CCACACTCCT 900 CCCTGTAAAA ATAACGGTGT CATTAAACAT GGACCGGCTG TTCCATGAGC TCATTCCTAG 960 GAAACAGTGG CTGAGTAGCA GAAGCCTGAC CGGTCTCCAT TTCCGCCCAA ATGTGGGATG 1020 TGTGCACGTG GCATAGAGCC TCGCACGTTG CTTTTGGGAG AATCAGCTTG AGTCAACTTC 1080 TGGCAAAAGA TTGGGGCCGT CTTTGGACAG ATTTGAATAT TAGACACCAT ATCATCTAAT 1140 GAAAACCAGC TGGGAAGAGT CAGTTTTCCT GTGTTCTTGG GCATTTGACA AATGGTGGGA 1200 GATAGTTCTA ATTTTAGAAA GGAAAACGTA ATGCATATTC TCATGATGAT TTGTCAACTG 1260 GATATTTTGC AGAGAGGAAA ACGTCTGAAA TGTCCCAAAT AAAGCTATCT GCTGTCATGA 1320 GAACACAGCT GGCAGGGCAG AAAGCAGTGT CGATCAACAG GAGGTCGTCC TGCACCGGGA 1380 CGTCAGTGCC CCGACACCTC GGTGTGTCCC TTGGCTGTGT GGCCTTGGGC AGGTCACTGG 1440 TCAAGCCTGA GATAATGACA TTGGTCTGCT GGGGAGCAGC GGCCCTAGGC CAGATGTACT 1500 AGGAGGCCCC TTCCTGGCTG TGATTTTAAG ATGGAGGGGA AAATGTTTAT TTGTTCTGTG 1560 AAAGCCAGGG GTGGGGTAGG ACAGAGCCAG CAACACCGAC AGCCCATCAT GCTGAGCCAG 1620 AGGTCTGCTG AGCTGAATTG AAGCTGTGTC AACTACAGTA CGTGCCTCAC CGAGCCTCAG 1680 TTTCCACATT GGTGCTGTGC AGATGATAAT ACAGACTTTG CAAGGCTGTT GAGACTTACC 1740 TGCACTAAGA CATAGAAAGT GCCCAACACA GCGCCTGCAG GGCCAGCACT CGGTGGCAGT 1800 CTAAGGAATG TCTGTCACAG CGCTCCCAGA TGGCAGGTCC TGCCTGCCTG GGCCCAGCTC 1860 TGGCTGTGTG GCTCAGGACT ATGGGACCTC TGCAGGCTGC GTCCCCTGCC TGCCTCAGTT 1920 TCTGCGTCTA AGCTAGAAAG CATGATTGTT CCTCCCCGTG GGGCCGTTAC GAGAAGCAAG 1980 CACATGGAAG CGTGCCAGGC ATTTTCCGAA CGTCTGGAAC ATCCTCAGCG GCAGGGTCTC 2040 CTCCTCCCTC TCCTCCTCCT CACTTAGAAA TATTTTCCCT GGGAGTCCCA CGGAGGTCGT 2100 GAAGATGACA GAGGCTGCTG GCACTAACAG CTGTGTGGGG CAGCCCAAGC CCCTACTTTG 2160 AAAGTTCCAT TCCATCCCTC GCATTTCATC TGAAGAGCGC TATGTTCTCC CTGGGGAGAA 2220 CTGGCCTGTT GCATATGAAG AGTCCAGAGA TTTTGAACAA GGGAACCCCT TCAGCTTCGA 2280 ATGACCATTA CCGTTGATGA TCCCAGAAGT TCCCTTTCCA AGCAGTGACC CATGGACTTG 2340 TGTCCCTCGT GTGATAACCT GCACTACACA CATATCCTAC AAGTGTCCAT AGTGGTTATA 2400 AGCTGCCACA GCCATACAGA TCTGAGAGCC AGAGGCCTTC AAACCAGCTA AGGCTCTGAA 2460 ACACTTCAAC TCCACTTAAG AAAACAAATC GGAGCACATC CGTGATCCCA CAAATGCTAA 2520 TTTGCTTGTC ACACATCAGA AACCCAGGAA GGCACAGAAT AGATGCTCTC TTACTGGCTT 2580 ATAGGTTGGG TACTTTAAAG TTGGAGACGT TTAAATCAGA GATAAACCTA TTGTAACAAT 2640 ACATTTCATG TCATGTGAGC CTTTTGTCTT CCAGCAACTA AAGGGAACTG TGGTAGGATG 2700 AGCTGGGGTC ACAGGGACAA GGAAGACAGG TAAGGGGACG GAAGCCGGGG CAGCAAGGAG 2760
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