Tag | Content |
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EnhancerAtlas ID | HS187-05372 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:11964970-11966870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:11966522-11966540 | CCCTCCCTCCCTCTTTCC | - | 6.03 | ZNF263 | MA0528.1 | chr12:11966190-11966211 | CTTCCCTGCCCCTCCTCACCC | - | 6.16 | ZNF263 | MA0528.1 | chr12:11966536-11966557 | TTCCTTCTCTTTTCCTCCCCC | - | 6.21 | ZNF263 | MA0528.1 | chr12:11966522-11966543 | CCCTCCCTCCCTCTTTCCTTC | - | 6.49 | ZNF263 | MA0528.1 | chr12:11966518-11966539 | CCCTCCCTCCCTCCCTCTTTC | - | 6.79 | ZNF263 | MA0528.1 | chr12:11966514-11966535 | GCCTCCCTCCCTCCCTCCCTC | - | 6.86 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_01754 | chr12:11965086-11966647 | Aorta | SE_04644 | chr12:11964094-11969016 | Brain_Anterior_Caudate | SE_08728 | chr12:11963863-11969448 | Brain_Inferior_Temporal_Lobe | SE_09138 | chr12:11956651-11968946 | CD14 | SE_12879 | chr12:11962849-11967639 | CD34_Primary_RO01480 | SE_13315 | chr12:11956663-11969343 | CD34_Primary_RO01536 | SE_14048 | chr12:11962831-11967308 | CD34_Primary_RO01549 | SE_25354 | chr12:11962884-11969225 | DND41 | SE_25772 | chr12:11962822-11967446 | Duodenum_Smooth_Muscle | SE_30906 | chr12:11962936-11968622 | Fetal_Thymus | SE_32609 | chr12:11962672-11967045 | GM12878 | SE_38246 | chr12:11964251-11968325 | HUVEC | SE_39367 | chr12:11962935-11968406 | Jurkat | SE_46110 | chr12:11965036-11968111 | Osteoblasts | SE_49833 | chr12:11962956-11969294 | RPMI-8402 | SE_51050 | chr12:11965023-11966910 | Sigmoid_Colon | SE_51622 | chr12:11964133-11966805 | Skeletal_Muscle | SE_54310 | chr12:11964137-11967087 | Spleen | SE_58379 | chr12:11878906-11990784 | Ly1 | SE_58935 | chr12:11959439-11993441 | Ly3 | SE_59811 | chr12:11956477-11992634 | Ly4 | SE_61133 | chr12:11961570-11993572 | HBL1 | SE_66238 | chr12:11962935-11968406 | Jurkat |
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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 |
GH12I011808 | chr12 | 11961695 | 11968582 |
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Enhancer Sequence | TAACTCATTT TAAGCCTTGG TTTTAGTCTA CCTAAAATTT ATAGAACACT GTAAAATATG 60 CTACATGTAA TAAGATATTT ATTAGGAGTC TTCTTGCACT TGTTCAGAAT GCTTTTTATT 120 ATGTTTCTGC TCATTATTGT AGATATTCTC CCATTTTGGA GAAATTGACC GCGTGCACAC 180 TCTTCACTGG AGTTTTGCAC AAATCTTACC AGAAAACTGG TGAAGATCAG TCCTGAGGCC 240 CCTTCCGCCT CTAATTCCTT GCAGTATTTT GGCTGTACTA TGTGCTGTTA CACTAGATCA 300 CAATAAGCAG CTGCCAGTTT CCTCACAGGT TCCCTTGGGG AAGGATATGG GAATAATTCT 360 TAGGAACCCC CCACAAATTA TAGCAACCAA TGCAGTAAAA CCCCTTTAGC TCACTCCTCC 420 CCCTGTGCTC ACTCACATAC TCAAATATAT TTAGTGCTTT CCTTCCTCTC ACTCCGACAC 480 TTTTGGGAGA GCCCTGGGGG TGGTTGAGTA CCTTGTCCTT GGGTGGATTT TCTTGTTTTC 540 TGAGACTGGC TGCCATCAGA CTTCGGGAGA GGATCTTACC AGAGGCGGGT CTCTTCTTCC 600 CCCGCCACCG CCCTCAGTAT TCTTTCACAG CCACCACAAA GCCACGCTTT CTCTGCTAAG 660 TACACATTCC TAGGACTGTA ACAAAAGGCT TCTGTGAGTT TGAAAGCTGC AGGGGAGGCT 720 CCTGCGTGAA GGCCTAAGAT TTAAAGGGTT TCATTTCTCC TGTGCTGGGG ACTGTATTGA 780 GTGCAGTTTG AAATCTGCTT CACCACCACA AGGGGAAATA GAAATCAGCC CTAAAGCTGC 840 ATGGAGACCC CGGCTGGTCT TTATCCTCAT AGCTTAGTGA TTTCCTGCCA CCCAAGAGGC 900 AGTGAGGGGC TCCCTGACAT TCCGGAGGCC CCAGGAACCC TGGCTGCGGT GACCCGGTGC 960 TGGGGAGGGA GTGCATGGGG TAGGCTCCTG GTTGTGAGCC TTCAGTTCGC CGGGATGTCT 1020 ATGCTGTGCT GTGTGGCTAC TTAGCCAAGG CTGTGCATGC CAGCCGGAGC CAACAGCTTC 1080 AGCAAACCTG CCCTCCGGGG AGAGTGGATT TCATTGTTTT CAAAGAGATA CAGGAAATCA 1140 GAATTTTCCA TCCTTCCATG GAGAGACTTG GATTGGACTG AGAAGAGAAC CAGCATTAAA 1200 AAGGAAGTCT CCTTCCCTTT CTTCCCTGCC CCTCCTCACC CCAGCCCCAG CCCACCCGCC 1260 AGGGGCACAC CCTCCCTCTG CCGGCCTTTG GGTGGAAACC TTCCTGCCTG CAGCACAGGC 1320 AGTGTGAACT GCGGGGCTGT CTGAGCAACC CAGCTCTTGC CTTTTCAGTA GCAGAGGTAA 1380 TGTGGCCACG ACTCAGAATT ATGGGACCCC AGATGCTGAG GAAGTAAACT GACTTCTTTT 1440 CAGCTCACAG CAGACGCATA GACAACAGAG TAGATTTCAT GTTCTAATGA AACAGTGTAG 1500 AAACTCTGTC CTTGGTGGCT CAGTACTGTG TGGTATGAGC CTCTGCCTCC CTCCCTCCCT 1560 CCCTCTTTCC TTCTCTTTTC CTCCCCCACC CCTTCACGGC CTGCCCTTTC CTGATTCTTC 1620 AGAACTGACA ACTATAAATC CAGCCCAAAT TCCTTTAAAC AAAGGGTCAC CAAGAGCACG 1680 ACCTTGAAAA GACTTCTTGT GATATGCACT TGCAGAGTTG CATATTGTTC CTTGGATTTA 1740 GGACAGGCCA AAGAAATCTT CCACTTTATT TAAGAAGAGC CTGTGTGGTT CGAGGCCAGG 1800 GCCGTGGACA TAGGATTAAC CACAATAATA ATACAATGAA GTACACATGC AAAATGAAAA 1860 CTTAATAATG AAGAACTACT GATTTTTTCC AGGGAGTATC 1900
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