Tag | Content |
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EnhancerAtlas ID | HS182-09349 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:37038800-37041060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr17:37039636-37039657 | AATGTAAAAATGAAAATAAAA | - | 6.14 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_04550 | chr17:37038743-37040683 | Brain_Anterior_Caudate | SE_06121 | chr17:37035628-37039853 | Brain_Hippocampus_Middle | SE_08151 | chr17:37039508-37040883 | Brain_Inferior_Temporal_Lobe | SE_12286 | chr17:37039814-37040741 | CD3 | SE_17169 | chr17:37039791-37040699 | CD4p_CD225int_CD127p_Tmem | SE_19419 | chr17:37039430-37040774 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20407 | chr17:37039442-37040798 | CD56 | SE_22571 | chr17:37039429-37040791 | CD8_primiary | SE_23506 | chr17:37038822-37039392 | Colon_Crypt_1 | SE_23506 | chr17:37040082-37040641 | Colon_Crypt_1 | SE_24046 | chr17:37040338-37040647 | Colon_Crypt_2 | SE_26978 | chr17:37039458-37040652 | Esophagus | SE_27795 | chr17:37039457-37044351 | Fetal_Intestine | SE_28678 | chr17:37038937-37044257 | Fetal_Intestine_Large | SE_30529 | chr17:37039524-37040779 | Fetal_Muscle | SE_31106 | chr17:37038707-37039393 | Fetal_Thymus | SE_31106 | chr17:37039575-37040805 | Fetal_Thymus | SE_31542 | chr17:37038684-37039380 | Gastric | SE_31542 | chr17:37039545-37040641 | Gastric | SE_42353 | chr17:37038710-37040910 | Lung | SE_48905 | chr17:37039513-37040717 | Right_Atrium | SE_50172 | chr17:37038691-37040817 | Sigmoid_Colon | SE_52400 | chr17:37038709-37044606 | Small_Intestine | SE_53492 | chr17:37038772-37040744 | Spleen | SE_55164 | chr17:37038966-37039416 | Thymus | SE_55164 | chr17:37040017-37040633 | Thymus | SE_59348 | chr17:37019329-37056453 | Ly3 | SE_62887 | chr17:37023359-37058235 | Tonsil | SE_65628 | chr17:37039824-37040664 | Pancreatic_islets | SE_68729 | chr17:37038789-37040792 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 37039761 | 37040627 | chr17 | 37040844 | 37040942 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I038876 | chr17 | 37032836 | 37043967 |
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Enhancer Sequence | AATTCTTTCT TGAAGCTTCT GGGTGGGTGG AGTGAGCCTG CTCTTGGTGA GAGAGATATT 60 TAAGAGAGAT ATTTATGCCC TCCATTACTT GTTTTGTAAA CTGGATTTTC CAAAAGTGGG 120 GCAGATCAGT CCACACGCCC AGGCTTAGCA TAAACCTGCA TCGTTGTCTC CCTGCAGATA 180 GTCTAGAGTA CTGCCTGTTC CCTCCTCTTT AGGGCCCTAC TGACAGGAGG CAGGGTTGCC 240 AGCCAGGGAA ACCAGCTTGT GAGGTGTCAA GTGGGAGGTG GGCATGGGCT GGGGAAGGAA 300 AATTGGGGGA CTTGGTTGCA CCTTTCCCCT CTTCTCTGAC TGCACATATT TGGGGTTCAT 360 TCTCCAGTTT CCTTGAGCTG TGGGGTAAGG ACTGAGGAGG GTAAAGATGT CCCTGATTCT 420 GGGGAGCCAG GAACTATGTT TCTGCCCCTT CCCTTAGGCA TCAGATGGGA GTAGGGTGTG 480 GTCTGTGTCA GACAAGGCTG GGTGCTTAAG TGTCTCTGGA TTCTAGCAAA CTGTCTTTAA 540 TCCCAGCTGC TTTTAAAAGG TGGGGCAGGG TTGGGTGCAG TGGTTTATGC CTGTAATCCC 600 AGCACTTTGG GAGACTGAGG AGGGTGGATC GCTTGAGGCC AGGAGTTCAA GACCAGCCTC 660 ATCTCTACAA AAAATGAAAT AAATTAGCCG AGTGTGGTGG TGTGGGCCTG TGGTCCCAGT 720 TACTTGGGAG GCTGAGGCAG GAGGATTACT TGAGTCTGGG AGGTTGAGGC TGTAGTGAGC 780 CCTGATTGCA CCACAGCACT CCAGCCTGGC AACAGAGGGA CACTCTGTCT CTAAAAAATG 840 TAAAAATGAA AATAAAAATA GGTGGAGCAG GAGTAGGCAA ACCCCGCACT GGGGCCCAGG 900 GCTTTCCCTC CTTCCCAAAA TTGTCTGCCT CTAACTGGAA AAATGGGGAC TAGGGATGAC 960 AGTGTGGGGG AGGGCAAGTG CAAATGGCCA GCCCAAGTAG CCAAATGTGG CCTCCAGGTA 1020 GCCCTCCCAC CTCACTTACC CCCAAATCCC TGTCCTTCAG GCCTCCTGGA GCCTGAGGGA 1080 TCACTTTGCT TCCTAACACC TACGTTTTAC AGATGAGGAA ACAGGCCCGC GTTTCCATGC 1140 CTTACTCAAC TTGCAGAATT GTTTCTCTTC TATATTACCG ACAGGGGCAG GCTTTTTTTT 1200 TTTTTTTTTT CTTTTCATTT TGTGTGCAAT CTGATGGCTG GTAAGTTCTT CCTCAAGTCT 1260 AGCCTTGATC TTTTTGACTG CTCTTTTTTT TCCTCTGATT GAACAATGCC TCCTTGTTGC 1320 TTCCTATCGC CACCACTTCA GCCCCTTAGG CCTGAGGGGA TGGACGGGTG AGAAACTGGG 1380 TTAGCAGGGA GCCCTCCCTT CCCGCCTGTG GGCAGCCTTC CCAGTAGGGG CTTTTGGAAT 1440 CCGCAGCTCT TTCTAGAGGC AGGATGTGGG GGCTGTTTTT TTTTTTTCCT TTTGGTAAAA 1500 CCAAAAGCTC CTTGTTGCTT TTGTTGATGT CTTTTTGTTC CTCCTTGAAC ACAAAGCTGT 1560 GGTTTTTGAA GAGATCCAAG CCTGGAACGG GCGAGGCTCT GTGTAGAAAG GGCGCTGGGC 1620 TTTCGGGTTC GCTATCCTGT TCTTCTGACC CTGGAGTGTG GCTGATGGCA GGACTGGAGA 1680 GTGAGGCTGG TGGCTGACAA GCTGTCCCTG TCACCTGTGA GCCCGGAAAC CTTGCCCCTG 1740 TAGTCCCACC AAGCAGGAAG GCCACCCAGA GGTCCTCACA GATAACCCCT CTCCTGGGAC 1800 ACAGGGCCTC TTCAGTATCA TATCCTTTTT TTTTTTTTTT TTTAATTTTT ATTTTTTGAG 1860 ACAGAGTTTC GCTCTTGTTG CCCAGGCTGG AGTGCAATGG CGCAATCTTG GCTCACTGCA 1920 ACCTCTGCCT CCTGGGTTCA AGCGGTTCTC CCGCCTCAGC CTCCCAAGTA GCGGGGATTA 1980 CAGGAGGCCG CTACCATGCC TGGCTAATTT TTTTGTATTT TTAGTAGAGA CGGTGTTTCA 2040 CCATGTTGTC CAGGCTGGTG TCAAACTCCT GACCTCAAGT GATCCGCCCA CCTCAGCCTC 2100 CTAAAGTGCT AGGATTACAG CGTGAGCCAC CACGTCCGGC TTTTTTTTTT TTTTTTTTTT 2160 TGAGATGGGG TCTCTCTCTG TCTCCCAGGT GGAAGTGCAG AGGTGTGATC TCGGCTCACT 2220 ACAACCTCCG CTTCCCGGGT TCAAGGGATT TTCCTGCCTC 2260
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