Tag | Content |
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EnhancerAtlas ID | HS148-15892 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr6:111910230-111912460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr6:111912036-111912047 | TGCTTTGTTTT | - | 6.02 |
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| Number of super-enhancer constituents: 41 | ID | Coordinate | Tissue/cell |
SE_00043 | chr6:111905012-111917090 | Adipose_Nuclei | SE_01477 | chr6:111910673-111911134 | Adrenal_Gland | SE_01477 | chr6:111911334-111913434 | Adrenal_Gland | SE_01892 | chr6:111910292-111913394 | Aorta | SE_02609 | chr6:111910127-111911825 | Astrocytes | SE_02609 | chr6:111911848-111913962 | Astrocytes | SE_24555 | chr6:111910660-111911012 | Colon_Crypt_2 | SE_24555 | chr6:111912196-111912740 | Colon_Crypt_2 | SE_25836 | chr6:111908800-111915284 | Duodenum_Smooth_Muscle | SE_26930 | chr6:111910177-111915191 | Esophagus | SE_28180 | chr6:111910460-111911278 | Fetal_Intestine | SE_28180 | chr6:111911629-111913739 | Fetal_Intestine | SE_29422 | chr6:111910287-111911511 | Fetal_Intestine_Large | SE_29422 | chr6:111911623-111915197 | Fetal_Intestine_Large | SE_31696 | chr6:111910285-111911137 | Gastric | SE_31696 | chr6:111911351-111913438 | Gastric | SE_33474 | chr6:111910290-111915988 | H2171 | SE_36399 | chr6:111909247-111914904 | HMEC | SE_36956 | chr6:111908817-111916894 | HSMMtube | SE_38953 | chr6:111910082-111915170 | IMR90 | SE_41014 | chr6:111910426-111911290 | Left_Ventricle | SE_41014 | chr6:111911970-111913660 | Left_Ventricle | SE_42404 | chr6:111910215-111911077 | Lung | SE_42404 | chr6:111911171-111913478 | Lung | SE_44157 | chr6:111908814-111915968 | NHDF-Ad | SE_44783 | chr6:111910076-111915214 | NHLF | SE_45702 | chr6:111908728-111916180 | Osteoblasts | SE_47224 | chr6:111907764-111917003 | Panc1 | SE_48418 | chr6:111910133-111913940 | Psoas_Muscle | SE_49187 | chr6:111911244-111913429 | Right_Atrium | SE_50264 | chr6:111910257-111911154 | Sigmoid_Colon | SE_50264 | chr6:111911360-111915118 | Sigmoid_Colon | SE_51251 | chr6:111909320-111914248 | Skeletal_Muscle | SE_52070 | chr6:111909440-111915027 | Skeletal_Muscle_Myoblast | SE_52559 | chr6:111910287-111911113 | Small_Intestine | SE_52559 | chr6:111911237-111915118 | Small_Intestine | SE_54880 | chr6:111910427-111915136 | Stomach_Smooth_Muscle | SE_55947 | chr6:111908993-111914469 | u87 | SE_63870 | chr6:111909299-111915041 | HSMM | SE_64317 | chr6:111908912-111915049 | NHEK | SE_67791 | chr6:111908993-111914469 | u87 |
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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 |
GH06I111587 | chr6 | 111909054 | 111916685 |
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Enhancer Sequence | AATTTTGGGA GTGACCAAAT ATTATAATGA TCAGAAAAAT TATCTTTTTT TTTTTTTTTT 60 TTGAGATGGA GTCTCACTGT GTCATCGCCC AGGTGCAGTC TCGGCTCACT GTAACCTCTG 120 CCTCCCAGGT TCAGGCAATT CTTGTGCCTC AGTCTCCCGA GTAGCTGGGA TTACAGGCGC 180 CCGCCACAAC AACTGGCTAA TTCTTTTTGT ATTTTTAGCA GAGACAGTGT TTCACCATGT 240 TGGCCAGGCT AGTCTCAAAC TTCTGATCTC AAGTGATCCA CCCACCTTGG CCTCCCAAAG 300 TGCTGGGATT ACAAAGTGGG GTGAGCCACC GTGCCTGGTG AAAACTTACC TTTAAATACA 360 GATAACAGAA TGTTAAAAAG TAGTTTATGG TATTATTCTC ACAAATTACT CCTTTTAAAC 420 CTGGCAATCA CTGAGAAATA CAGCCTTGAC CTTGCCAACA TTCAGTTCTC AGTGATTCAT 480 ACTTAAGGGA ATCCACCACC ACACCCACCC TATGACTGGG CGCTTAGAGC AGGGGTGGCA 540 TCCATGCACT CCCACTCTGT TGACTTCCCA GCATTTATAC ACCACGTCCC AGTTTTAGGC 600 ATCAGAGGCT CTTTCTCCCG CTCCAGCCCA AGGCCCCATT CTCCTTACAC CCTCCTGCTT 660 CCCCAGCCCC TGCCCTCATT CCTGATCTCA CACTCATTCT TACCTATTTC TTCCAAGCAT 720 CTTCTAAGTT ACATTTCTCT ATCTCCTCTT TGTTTTTTTC TTTTTTGAGT TATGAATTAC 780 TGTGTTGCTC TCTTCACTTT AGGAAGCTTT ATACTTAGTA TACATGTACT AATATGTAAA 840 TTATGGTTGA TTACAGCATT TGTAATTATT TCTATAATTT ATTTTAAAGC TGCGCATCAG 900 GCCTTTGGTC AGGCACTTCT TACACTCTGA ACTACTTTCT GTCCAGTGTT TATTTGCTAA 960 GAAAAATATC AGGCCTCACA GCCCTGTGTT TCATCTGTAA AGCCCTTTTG TTATTTTCCA 1020 GTGGCCTCAG CGGAGATTTA ACATCAAGAA TGGTAGTAGG AAAAAAAAAA TGGTGATAGA 1080 ACCTTTTATC TCAACCTAAG ACTTATCACT TTCAGAGATG CTTCCTGCAC TGATACATAT 1140 TATTATTTCG GAAGTAGTTT ATTGAGAGTC TAGTATGTGC CAGACACTGT GCTTAAATCC 1200 TGGGGAATTA TGAATTGAAA GTACACGTTT GCATTTGCAG ATGCATAAAA ACTTGCAGTC 1260 TAGAAGGAGA GGAGACACGT ACATAATTAG ATGCCATGCT GGTGTTAGGT GTCCCAACAG 1320 GGCCAGAGCA GGAGGGAGAC AGAGGCCCTG AAGGAGAACG TGATCTGGGG AGGTTTCCAG 1380 AGGGACACTT GAGCTAAGTC TCAAAAAATG TGTATGATGG TGGTTGCATA ACTCTGTAAA 1440 TATACTAAAA CTTATTGAAT TTTTTATTTA AAATGGGTTA AGGGTAAACC TTGCAGTATG 1500 TATATTAGAT CTCGATAAAG CAGTTTTTTT AAAAGGTGTA TTGAAACTGG GTCAAACACA 1560 CCAGAAGGGG AAGAACATCC CCAAGAGAGA GAAGAGCCTG GCAAACGCAT GGAGATGTGA 1620 ACCATCGCGA CAAGTAGGGG GACTGCCAGT CTTAGAGTGG CTGGAATGTA GGGTAGCTGT 1680 GGATGGCTCA AGTGTCCAAA AGGATTTAAG CAGCAAAATC ACAGAAACAA CTTCATTTTC 1740 ATGTAATGGC CCGAATCCCA GAGTCTCAAT GACATTCTGG GCACCTTCTG GTTTTTTGTT 1800 TTGTTTTGCT TTGTTTTTGA CTAAAAGCCC TTTCTCTGCC AAGTCTAAGA TGGGGAAGAA 1860 AGATGACGAG AAGGAAGAAC CCATATGCCC AAAGATTAGA ACAAAAAATA CATTTTCTAG 1920 AAATCATTTT GGTCATCTCT CTGCTTCTAG GCAGGTTTGT TAAACTAACC CAGACAGAGG 1980 AACCCATTTT GTCCTTAAAG GTCCCTAGAG AAGGAGACTC CAAGTGGGAC AGGCTTTAGG 2040 CTAAGAAAAA GCATTCTCTG CAGGCCCTTT GCAAATCCAG CCACACATGG AAAGCCCCTA 2100 AGAGAAGCAG AATGCCCTCC CTGCATTCTG ACCTGTTCAT GCCAGCCTAG TGACACGAAG 2160 CATTGATGTG AGGCCCTTGT TTCTTCAGTC ACCCAGCCCA GAATGCCCAG AGGAGGTAAA 2220 GATCACTTAC 2230
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