Tag | Content |
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EnhancerAtlas ID | HS103-00124 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr1:12243710-12245560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:12245361-12245382 | TTTTTCTTTTTCTTTCTCTTT | + | 6.77 | ZNF263 | MA0528.1 | chr1:12245259-12245280 | CCCCTCCGCCACCCCTCCCCC | - | 6.22 | Znf423 | MA0116.1 | chr1:12245459-12245474 | GCACCCCTGGGTGCT | - | 6.35 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_00369 | chr1:12226565-12247198 | Adipose_Nuclei | SE_01471 | chr1:12243922-12246504 | Adrenal_Gland | SE_04546 | chr1:12243735-12246962 | Brain_Anterior_Caudate | SE_06521 | chr1:12243738-12246994 | Brain_Hippocampus_Middle | SE_09154 | chr1:12224797-12249846 | CD14 | SE_10696 | chr1:12243928-12245111 | CD19_Primary | SE_14553 | chr1:12243811-12245422 | CD4_Memory_Primary_7pool | SE_17827 | chr1:12231021-12246713 | CD4p_CD25-_CD45ROp_Memory | SE_18389 | chr1:12226183-12250288 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19117 | chr1:12243746-12249924 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20048 | chr1:12243749-12245373 | CD56 | SE_20873 | chr1:12243794-12244892 | CD8_Memory_7pool | SE_22347 | chr1:12243335-12245917 | CD8_primiary | SE_26251 | chr1:12243680-12246989 | Duodenum_Smooth_Muscle | SE_27503 | chr1:12243903-12246642 | Esophagus | SE_30788 | chr1:12243698-12246708 | Fetal_Muscle | SE_32030 | chr1:12243891-12246634 | Gastric | SE_38661 | chr1:12243533-12246545 | HUVEC | SE_41498 | chr1:12243811-12247059 | Left_Ventricle | SE_42336 | chr1:12243813-12247305 | Lung | SE_48967 | chr1:12243799-12246749 | Right_Atrium | SE_50250 | chr1:12243815-12247081 | Sigmoid_Colon | SE_52522 | chr1:12243745-12249859 | Small_Intestine | SE_53313 | chr1:12243756-12247385 | Spleen | SE_55394 | chr1:12243888-12244461 | Thymus | SE_55394 | chr1:12244622-12245112 | Thymus | SE_61096 | chr1:12184746-12245090 | HBL1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 12243852 | 12244671 | chr1 | 12245348 | 12245387 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I012182 | chr1 | 12242459 | 12247879 |
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Enhancer Sequence | TTTTATCTAT CTATCTATCT ATCTATCTAT CTATCTATCT ATCTATCTAT CTATCTATTC 60 TATCTACCTA TCTATCTATC TATCTATCTA TCTATCTAGC TAGCTAGCTA GCTAGCTATC 120 TATTCTATCT ACCTACCTAT CTATCTATCT AGCTATCTAT CTATTCTATC TACCTATCTA 180 TCTATCTATC TATCTATCTA CCTACCTACC TACCTACATA TCTATCCATC CTCTCCGATT 240 CCCTCACCAC TGGGTCTCAG ATTCCCTGCC TGTTAAATAA ATGGTCAGTT AACCCTCAAC 300 AGTGATTTTC AATTTTTCAC TTGAGGCCCC CATATTTTGG AAGATTGTAG TTTGCTGAAC 360 ACGCTGACTG AATCAAGTAC TATCCAACTT ATTTCCTCAT TTTAACATGT CAAAGATCCC 420 CTGTGGGGTG AGTGGGGTGT GAATTGGAGC CTCCCCAATC CAAGGCACAG GAACTGGAAG 480 CTTCTGTAGC CCTGCATTTC CTAGAGAATG CTTGCCATGT TTTGGGGACC TCCTGGGGGG 540 CCCCTGTACT GACCAGAGGC CGGCTCCCAG GGCTGTGGTT TGGGCCCAGC CCCCTGCTCC 600 TGGGGACTGC TGCTGTGGAG GGAGTGACCT TTTGTTCTGC TTTGCCAAGG GGCTTTCTGT 660 TCCTCATTGT TTAGCCATGA CAAGGCTGTG GATTTTTTTT TTTTTTTCTG TCCAAGAGAA 720 TAAACAGGCC TGAGATTGCT CAAGGGAGCC GACCCCCTCT GCCAGCTACT GGGGGCTGGA 780 GGCTCACAGA GCCAGGGAGG AAGTCCTACC CCCTCTGCCG GCTACCGGGG GGGCTGGAGC 840 CACACAGAGC CAGGGAGGAA GTCCAGGGAC GGTCACTCAC AGCAAAGCCT CAGACAAGAG 900 AGGAACCTGG AGGGGAGGAG GTGGGAGGCC ACCACTCAGC CGGCCTGGGG GCCATGGGAG 960 TCCAGCTGCC TGCCGTTAGT GGCCAGGAGC CCTCGTCCAT TGCGGCTCTT GAGAGCCCAA 1020 ACTTGGCCAC GGCAGGGCTC TTTCCCATCA GGCCCTTTGA GCCCTGATGG GAAACCCTTC 1080 CCCAGCCAGG GTGGGATTTC TTGCTGCCGC CTGGAGCCGC CCTGGCCCTG TGGTTCTCAG 1140 GCCCTGGAGG AGTGAGGGGC TCCCCTGGTT ACCCCAAGGG CACTCGTGGG GATGAAGCCC 1200 GCGGGATGCA GGATTCCCAC GAGACCTGTG CTGGCCACTG TGCGGGGTGG GGGGCTGCCA 1260 GGGAAGAGGT GCAGCCCCTG CCTGCCTCAG GGATGCGATC TGAGGGAAGA GGCAGCTGTG 1320 TCTGGGAGGC CGTTCGGTCG GAGGGGGATA GGCACAGCCC CTGCCCTTGG GGAAGCGCCC 1380 AGCAGCAGCC TTCAGGGAAG GCAGTTTGGG GGTTTGCCGA GGGCCAGGAA GACCCTCTGC 1440 CGCAGTTAGT ATTCGATGGA ATGGCTTGTG CAGAGGGAGC TGCAGAAGCT GCCATTTCTC 1500 TGGGTTAGGG GCTCCCACAG CCTTTGGATG CCGGGTCTCG GCCATGAGCC CCCTCCGCCA 1560 CCCCTCCCCC AGGTCACCTT GCTCAATCCA GGAGGCCGGA TGATCAGAGT GTGTTCTGCA 1620 AAGGAGCGTG AGAATCACTG GGGAGATTTC CTTTTTCTTT TTCTTTCTCT TTTTTTAATG 1680 GTACAGCTTC CTGGGCCCAC CCCTGAGATT CTGCACTTGT TTGGGGAGTG GGTGTTGGCT 1740 TCATGACAGG CACCCCTGGG TGCTTTGGAC ACAGGCAGTG AGCTCCCCCC ACACTGTGTG 1800 AACCCCTGAG AAGGCTTCTC CTTTTGTCTA GGGTGCCTGG GAGTCTGCTC 1850
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