Tag | Content |
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EnhancerAtlas ID | HS103-26255 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr9:139420180-139422660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr9:139422299-139422309 | GGTGCCAAGT | + | 6.02 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00323 | chr9:139418153-139429355 | Adipose_Nuclei | SE_01312 | chr9:139420602-139421547 | Adrenal_Gland | SE_03738 | chr9:139420036-139421287 | Brain_Angular_Gyrus | SE_04058 | chr9:139419277-139424589 | Brain_Anterior_Caudate | SE_05120 | chr9:139419016-139427605 | Brain_Cingulate_Gyrus | SE_05830 | chr9:139415026-139429430 | Brain_Hippocampus_Middle | SE_06959 | chr9:139419153-139422864 | Brain_Hippocampus_Middle_150 | SE_08378 | chr9:139419137-139422426 | Brain_Inferior_Temporal_Lobe | SE_23278 | chr9:139419344-139424601 | Colon_Crypt_1 | SE_23785 | chr9:139419354-139422961 | Colon_Crypt_2 | SE_24688 | chr9:139419309-139430118 | Colon_Crypt_3 | SE_26827 | chr9:139420308-139422354 | Esophagus | SE_30179 | chr9:139419237-139422981 | Fetal_Muscle | SE_32032 | chr9:139420329-139421791 | Gastric | SE_32032 | chr9:139421868-139422742 | Gastric | SE_34452 | chr9:139420117-139425754 | HCT-116 | SE_41264 | chr9:139420032-139429262 | Left_Ventricle | SE_41775 | chr9:139422133-139423868 | LNCaP | SE_42178 | chr9:139419265-139429352 | Lung | SE_47602 | chr9:139420405-139421464 | Pancreas | SE_47602 | chr9:139421948-139422273 | Pancreas | SE_47602 | chr9:139422310-139422748 | Pancreas | SE_48804 | chr9:139419286-139422853 | Right_Atrium | SE_50167 | chr9:139419272-139429460 | Sigmoid_Colon | SE_52818 | chr9:139420260-139424579 | Small_Intestine | SE_54755 | chr9:139420323-139421465 | Stomach_Smooth_Muscle | SE_57110 | chr9:139420496-139422984 | VACO_400 | SE_65497 | chr9:139420004-139423167 | Pancreatic_islets | SE_68678 | chr9:139420113-139426629 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I136524 | chr9 | 139419275 | 139430501 |
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Enhancer Sequence | GTGGCAGTGG CCTGGGGGGG CCTTACCCCG AGGGGCTTGT GGAGGCTGGG GGTGGGGGTT 60 CCTGTGCGTT TCTCAGCAGC CAGCCACGCC CCTGTCCCAA AGGCCCGGGA GGCATCTGTC 120 TTCCCCGAAG GCTTTTACCC GTGACCACGG CTTGGGTAGA GAGAACGCAA AAGGGCCACT 180 CTGGCCGACC ATCTGTTGCC AGAAGCCAAA AGTCCCAAAC CAACTGGCTT AAAGAAAACA 240 CATGTCACCC CTTCCAAAGG GGCTCTGGGG AATTCACTCA GGCCTTGCTA CGGCTCCTGC 300 CAGCCCAGTG AGCGACGGGC ACAGCCCCGG AATGAGGCTC CCCCTCCTCC ATCCCATGTG 360 GCCGGTCACT CCGGGGCTGC AGCGACAGAC CTGCCTCTGC GGGCACCTGT TGGGAGGGCA 420 GACGTGGTTC CCACTGCATG CAGATCCAGT TACAGGCTGG CCGGTCCCCG AGGTGGAGCG 480 GCCGCTGGGA ACCCGTGGAG TGCACAGGCT GGGCTGGGCT GGGCTGTGGC CACAGGAGGG 540 GCGCCCTCCC TCCACATAAA TGCCCCATTG TCAGGCGGGA GTTGGCCACA GCTCCCGCTT 600 GGAGAAAAGG CCCTTTTTGC TTTCCCAGCC GCTGAAGTCG GCAGGGGGTG GGTACAGGAC 660 AGAGGGCGCT CGGTCATCAA AGCCGGGGCT GGAGGCTCCT CAGCCTGGCC CATGCAAGCT 720 GGTCCCCTGC CTCCCGGCCC CTCGAGGCTC CAAGGAGCGG GAAAAGCTCA CCTGCTGGGC 780 AAGACGGGGA GGAGGGGCAG GGGAGGCCCA TCCCACAGCT TTAGGGGACC CCAGAGGGGA 840 GACGCTGGAG GTCCGAGCCC CTAGAGCAGT CTCCCACCAA GTGCCCTGAG GTCACAGGAC 900 ATTGGCTGTC CCTGAATGGA CCACGACACT CTGCCCGGAC ACCGGGCCCC ACTCCCCACC 960 CTGAGCGCGG ACCCCAACGT GGAGGACTGT GGGAGAATCT GCCCAACCGG ACGCATCCCA 1020 GTTAACGAGG CTGTATCACG CCGGGCCAGC AAGAGGAAAA CACGCCCCAT AAATCAGGCG 1080 TCGGTGCTCG GACAAAGGGC GGCTGGGAGC AGGTGTCAGA CGTGGCGGCA GCTGCTCCCA 1140 GCGGGTGGGG CAGGAGCCCC AGCCGGAGGC CTGAGGAGGC TCCCGTGGGG GAATGCAGGC 1200 TGAGAGGGCC CATTGTCCGC CCCCACTCCC AGCCTGGGCA TCGGACACCA CAGGGAAGGC 1260 CCCTGCCACG GCCCCACAGC CACGGCTTGG AGGTTCCGTG AGACGCGCTA GCTGGGGGGA 1320 ACCGGGCCGA GCCTGGAGAA AGTTTTGAGC CAGGTGTGGG GGTCTGTGTG TGGGGGGCAG 1380 CTTTGGGCCC AGTCTCCCGC TGCTGCTGTG GGCAGCCTCC AGCCTGTGCC CGCCCCAGTC 1440 TGTACCTCTC TCCCACATGG CCACAGAGCT GGAGCACCCT ACAGACGGCG AACACCTGCC 1500 CTCCGCACAG CACCCAGACG TCCCTGAGAA GGTGGGAGGG ACCTCAGGCC TGCAGCATGG 1560 CCATGGCCAG GACCACCAGC CTGTGAGCAA ATCCTTCACA GCTTTGGCGC TGGCCACACC 1620 CCCGGTACCC GGGCCACTCT GTCTTCAATG CTGTCCCGGC GGCCAGGTGG GTGTGGGCCG 1680 CGAGGTGGGC GCCAGGGCTT GGCCGAGTGA GGTGGCACCC AACAGCTGCC GCGCCCACGG 1740 GGATCCTCAG GGCTTCCATG AGTGACCCGC ACCCCACCTT CCACCGTCCC CGCATCTCCT 1800 CCTATCAGGG GCGGTGGGGA GACCCCTCTG GGGCTAAAAA GTGAGGCTTG AGATAGGGAA 1860 CGCCAGTCTC CCCCGACTGG ACGAGAGAGC TGCCCTGTCC ACCAAGCCAC CCAGCTCTCG 1920 GGCTCCCACG GAGGAGACCC AACCCACGCC AGGTGTGCCC CCGTGGACTC CCCTTCCGTG 1980 CGTCCCTCTT AGGGTCACCC GGCACCTGCC TGTCCCATCC CCCACGCTCA GTGGCCTGGC 2040 GGCGCTGGGG TAACCTGTCC TATCTGGGCC CCCCGCAGGT GAGCGGCGGG CGGGGACTCC 2100 AGGAGGGCTG CGGGGGGAGG GTGCCAAGTG GCCCCGGCGC CTGCTGTGCC GCTCCCGCCA 2160 CCTCTACCGC CACCACTTTG TTCCCGCCTC AGTATTTCCA CTGTGCCACT CCCACCCTCC 2220 CTGCCAGGGC CGCTCCATGG AAATGCGACT CCAGAAAGCA GCAGGAGGCA GATGCTGCCG 2280 AGACCTTTCA CCCAGGACGA ATTCTAAATT GTGCTGTTTT CCTTTCTAAG CTAAGCGGCC 2340 ATCTGCCACC CCCAGGGGAC AGAAGACAGT TCCCTCCGCC CCAAAATGAG AAGGAGGGGT 2400 GAGAGGGACT CAGTGCGGGT AGGACTCACT CACTTCCTGC CCTCAAGGAG TTTATGGTCA 2460 TGCAGGGCCA GGGATGGGGG 2480
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