Tag | Content |
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EnhancerAtlas ID | HS092-25809 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:238577440-238580100 |
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 | TTTATTATAT TAAACGTAAT ACATGTTTAT TATAGAAAAA TAATAAGGAA AATTCAGGCA 60 ATAGTAGAAA ATAAAAATTA TGCCTCATAC TTGACCAAGC ACAATACCTG TTAACATTTT 120 GTTTATTTTT CTCCATTCTT TTATCTGTGA CTTTTTTTTA ACATAGTCTC AATTATGTGT 180 CTCTAAATAG CGCATTTTTA AAATCTCCTT TTTTTAAGGA AAGAAATAAG CGTAACTCTT 240 GTATCAAATG CTCTGTAAAA ATGTTTTAAT GGCCACAAAA TATGGCTTTG AGGATGCACC 300 ATCACGTCCT CACTTCCGTA TTGCTGGACA CTGAGGCTTT TGTGTTTGTT TACTGCGGTG 360 AATAGCATTG CAGTGAACAT CTTTAAGAGT GAGGTTTTTC TACTTCAAAT TATTTCCTTA 420 AATTAGAATA TTAGAAGTGC AATTTAAACC CCAAACCTAC AAACACGGTT AAGGACCTGG 480 AGCTTTGCTT TCCTGAAAGG GTGTATCAGT TTACACTTGC ATTTGTGTTG TCTGAGAGTG 540 TCTTGTTCAT CACAGGATTA AGTACTGTGA TTATCTCAGC TTTGTAAATT TGACAGCTAA 600 AAACTGGCAG CTAACTGATT CTTAGGTATC TCAAGTTCTT TTTCAAATCG TCAAAACGTG 660 TCTTAGAGTG AGTGTTGATA TTTTCTTGCT GATTTGTGGA TTGCTTATTA ACCTTTTTCA 720 TAGTTGTTGC AAATATTTTT TTTCAGTTTA GATTAGGAAC TGAATATCTT CCTCATGTCT 780 TTAAAGAAAT ATGCCTGACC AGGTGCTTGA TAACCCTAAA CGGAGTTTCC TGCCGGGCTT 840 TCTCTTGTAT GATGTTGAGG CCGTCACGGT TTGTTGAGCA GAGGAGTGAG TGCTAAAAGC 900 TGGAGTTCAG CAGAACCACA GTGATGCCTC CACCCCGGGT AAATGCTTAA CCACACTCCT 960 CCCTGTAAAA ATAACGGTGT CATTAAACAT GGACCGGCTG TTCCATGAGC TCATTCCTAG 1020 GAAACAGTGG CTGAGTAGCA GAAGCCTGAC CGGTCTCCAT TTCCGCCCAA ATGTGGGATG 1080 TGTGCACGTG GCATAGAGCC TCGCACGTTG CTTTTGGGAG AATCAGCTTG AGTCAACTTC 1140 TGGCAAAAGA TTGGGGCCGT CTTTGGACAG ATTTGAATAT TAGACACCAT ATCATCTAAT 1200 GAAAACCAGC TGGGAAGAGT CAGTTTTCCT GTGTTCTTGG GCATTTGACA AATGGTGGGA 1260 GATAGTTCTA ATTTTAGAAA GGAAAACGTA ATGCATATTC TCATGATGAT TTGTCAACTG 1320 GATATTTTGC AGAGAGGAAA ACGTCTGAAA TGTCCCAAAT AAAGCTATCT GCTGTCATGA 1380 GAACACAGCT GGCAGGGCAG AAAGCAGTGT CGATCAACAG GAGGTCGTCC TGCACCGGGA 1440 CGTCAGTGCC CCGACACCTC GGTGTGTCCC TTGGCTGTGT GGCCTTGGGC AGGTCACTGG 1500 TCAAGCCTGA GATAATGACA TTGGTCTGCT GGGGAGCAGC GGCCCTAGGC CAGATGTACT 1560 AGGAGGCCCC TTCCTGGCTG TGATTTTAAG ATGGAGGGGA AAATGTTTAT TTGTTCTGTG 1620 AAAGCCAGGG GTGGGGTAGG ACAGAGCCAG CAACACCGAC AGCCCATCAT GCTGAGCCAG 1680 AGGTCTGCTG AGCTGAATTG AAGCTGTGTC AACTACAGTA CGTGCCTCAC CGAGCCTCAG 1740 TTTCCACATT GGTGCTGTGC AGATGATAAT ACAGACTTTG CAAGGCTGTT GAGACTTACC 1800 TGCACTAAGA CATAGAAAGT GCCCAACACA GCGCCTGCAG GGCCAGCACT CGGTGGCAGT 1860 CTAAGGAATG TCTGTCACAG CGCTCCCAGA TGGCAGGTCC TGCCTGCCTG GGCCCAGCTC 1920 TGGCTGTGTG GCTCAGGACT ATGGGACCTC TGCAGGCTGC GTCCCCTGCC TGCCTCAGTT 1980 TCTGCGTCTA AGCTAGAAAG CATGATTGTT CCTCCCCGTG GGGCCGTTAC GAGAAGCAAG 2040 CACATGGAAG CGTGCCAGGC ATTTTCCGAA CGTCTGGAAC ATCCTCAGCG GCAGGGTCTC 2100 CTCCTCCCTC TCCTCCTCCT CACTTAGAAA TATTTTCCCT GGGAGTCCCA CGGAGGTCGT 2160 GAAGATGACA GAGGCTGCTG GCACTAACAG CTGTGTGGGG CAGCCCAAGC CCCTACTTTG 2220 AAAGTTCCAT TCCATCCCTC GCATTTCATC TGAAGAGCGC TATGTTCTCC CTGGGGAGAA 2280 CTGGCCTGTT GCATATGAAG AGTCCAGAGA TTTTGAACAA GGGAACCCCT TCAGCTTCGA 2340 ATGACCATTA CCGTTGATGA TCCCAGAAGT TCCCTTTCCA AGCAGTGACC CATGGACTTG 2400 TGTCCCTCGT GTGATAACCT GCACTACACA CATATCCTAC AAGTGTCCAT AGTGGTTATA 2460 AGCTGCCACA GCCATACAGA TCTGAGAGCC AGAGGCCTTC AAACCAGCTA AGGCTCTGAA 2520 ACACTTCAAC TCCACTTAAG AAAACAAATC GGAGCACATC CGTGATCCCA CAAATGCTAA 2580 TTTGCTTGTC ACACATCAGA AACCCAGGAA GGCACAGAAT AGATGCTCTC TTACTGGCTT 2640 ATAGGTTGGG TACTTTAAAG 2660
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