Tag | Content |
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EnhancerAtlas ID | HS120-00457 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr1:154399670-154401100 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr1:154400148-154400162 | CCCCTTTGATGTCT | - | 6.14 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00437 | chr1:154399481-154401751 | Adipose_Nuclei | SE_01040 | chr1:154399528-154400582 | Adrenal_Gland | SE_01040 | chr1:154400681-154401626 | Adrenal_Gland | SE_06653 | chr1:154399347-154403450 | Brain_Hippocampus_Middle | SE_09189 | chr1:154398672-154408855 | CD14 | SE_16173 | chr1:154399945-154400671 | CD4_Naive_Primary_7pool | SE_18405 | chr1:154399517-154407766 | CD4p_CD25-_Il17-_PMAstim_Th | SE_24531 | chr1:154399580-154400359 | Colon_Crypt_2 | SE_26130 | chr1:154399302-154401704 | Duodenum_Smooth_Muscle | SE_26877 | chr1:154399516-154400662 | Esophagus | SE_26877 | chr1:154400694-154402391 | Esophagus | SE_32086 | chr1:154399571-154400607 | Gastric | SE_32086 | chr1:154400656-154401897 | Gastric | SE_41139 | chr1:154399325-154402156 | Left_Ventricle | SE_41647 | chr1:154399531-154400535 | LNCaP | SE_41647 | chr1:154400745-154403911 | LNCaP | SE_42431 | chr1:154399355-154400656 | Lung | SE_42431 | chr1:154400696-154402137 | Lung | SE_47983 | chr1:154399591-154400258 | Pancreas | SE_47983 | chr1:154400922-154401243 | Pancreas | SE_48261 | chr1:154399318-154401864 | Psoas_Muscle | SE_48934 | chr1:154399344-154402194 | Right_Atrium | SE_50453 | chr1:154399516-154401315 | Sigmoid_Colon | SE_51380 | chr1:154399138-154401914 | Skeletal_Muscle | SE_52880 | chr1:154399518-154401631 | Small_Intestine | SE_54618 | chr1:154399097-154409137 | Stomach_Smooth_Muscle | SE_62668 | chr1:154357227-154415486 | Tonsil | SE_65390 | chr1:154399323-154400849 | Pancreatic_islets | SE_65390 | chr1:154400868-154402476 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 154399696 | 154400530 | chr1 | 154399716 | 154400696 | chr1 | 154400830 | 154400990 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I154427 | chr1 | 154399576 | 154401508 |
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Enhancer Sequence | GGTGTGAGGC CCAGCTGGGA CTCAGATTTT GCTGAGGACC AGGACAGTAC TGTGTGCTGT 60 GTCCTGGCCT TGCAGCAGTG AATGTGTCTC CCGTTTCTCA AGGGCAGGTC TCTGGGATGC 120 CTGACTGTGT CTTCCTTGCC AGTGCCTGGC TGCTGCAGCC TCCTCAAATG TTTATCAAAC 180 ACAGGACTTG CCCACCGTGG GAGAAAGTAA GGCCATAGGT GTCTCAGGAA CCTGCCCAAA 240 CTCGCCTGGC TGCACGGTGA CAATTCAACC AGCTTTCTTA CCCAAGGTCT GTTGGTGACC 300 AGAGAAAACC TTAGATGACC GGCTGCCATG ATGGCCTTAT ATCTGTCCCT TTTCTGCCAG 360 CCTTGAGGTA GAGGGTGCCA GGGAGGAGGA CTCTGGCTCT AGGTGTTAAA GTGAGAGGGA 420 AGTGTGAAGG GTATCTGTAT AGCTAGACAG GGCTCAATGC CAGGCAGAGC TGTCTCCGCC 480 CCTTTGATGT CTATGTCTCT GTCCCTGGAC TGTGGCCAGT AGCCAGTGTG GACTCCAACC 540 TCACCAGCTT TAGGGGTGTT ATCTGCCTGG GAGTCACTGA TCCTTACTCC CTCCTCTGAC 600 AGCCACCTTG GATGGGGTGA AAGGAAGGAC AGCCTGCCAA GTATGAGATA AAAACGCCTC 660 ATAAACAAGA AGGGATTTGC AGGCCAGGCA GAGAGCCTTG TGCTGCTTCT GAGTCCCAGG 720 AGCATGGGCG AGGAGGTGAG GTCAGGCACT CAGCAGCTGC TGGTCCTCTC TGAAATCTTT 780 GGCCAGATTT ATTGCTACTG CTTGCTAATA AATGGTTATG CATTTGGTTC AAAGGACCAA 840 GTGTGCTTAC ATGAAAACTG GCTGTGTTCC CTGGCCTCTG TTTCCTTAGC TGGTTGGACT 900 AATTTGATTG GTTAATAAAT GAGTCCAAGG TGGTTGGGCT AATTTTTATC TTAGATTCTA 960 TGACTCTATA ACTGCTACTC AAAAAAAGTG TACTTGTTCC TTTAATCTTT AATCTTATTT 1020 TTCTTGAGTA GTAGAATACA CCCAATTTTT TTCAAGGGGT AGAGAATGCA TTTTTTTTTT 1080 AACCTTCCAG TTTGGTCCCT AGAGTAAACA CAGCATTGCT GTAGTAGATG TAGGGTACTG 1140 GAGGGAGCAT GGAACAGGGA ACCAGAAGCC CTGGTTCCTA CCCCAGCTGG GCATCTGGGC 1200 CAGTCTCTTG ATTCCTCTGT GCCTCAGTTA CCAACTATAT AACGGGCATT CTGCCATGAA 1260 TACCCTGCGA TTTGGAAACC TCCTGTGTAC GTGTGCACTT GGGTGCCTGG CATTCATTCC 1320 TAATGGCATC CATTCGTTCA CACATTCATC CAGTACTCAG CAGACTCCTG CCATGGGCCA 1380 GGCAACGTCC CGGGCACTTG GAATATAATG GAGAACAAAG CAGGGTGCCT 1430
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