| Tag | Content |
|---|
EnhancerAtlas ID | HS178-01639 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr1:154399260-154401670 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr1:154400148-154400162 | CCCCTTTGATGTCT | - | 6.14 | | ZNF263 | MA0528.1 | chr1:154401281-154401302 | TGAGGAGGAGAGCGAGGGGAG | + | 6.42 |
|
| | Number of super-enhancer constituents: 30 | 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_19165 | chr1:154401205-154402489 | CD4p_CD25-_Il17p_PMAstim_Th17 | | 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 |
|
| | 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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I154427 | chr1 | 154399576 | 154401508 |
|
Enhancer Sequence | AAAAATATAT TGTTGAAGAT TCTGTGTGAA AGCTATACTG TAGTTGTGGC TTTTTATAAC 60
CCTTTCAAGC CCTCTGGGCA GTAGCAGTCC ACCCCTTATT GCCCTCAGTG GACTTCACCT 120
TCTAGGGACT CAGAATTTTT TTTTTTTTTT TGAGACGGAG CTTCGCTCTT TTTGCCCAGG 180
CTGGAGTGCA GTGGCGTGAT CTCGGCTCAC TGCAAGCTCC GCCTCCCTGG TTCAAGCAAT 240
TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ATTACAGGAG CCTGCCACCA CGCCCAGCAA 300
ATTTTTTGTA TTTTTAGTAG AGACAGGGTT TCACCATGTT GGCCAGGATG GTCTCGATCT 360
CTTGACTTGT GATCCGTCTC GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGTGTGAGGC 420
CCAGCTGGGA CTCAGATTTT GCTGAGGACC AGGACAGTAC TGTGTGCTGT GTCCTGGCCT 480
TGCAGCAGTG AATGTGTCTC CCGTTTCTCA AGGGCAGGTC TCTGGGATGC CTGACTGTGT 540
CTTCCTTGCC AGTGCCTGGC TGCTGCAGCC TCCTCAAATG TTTATCAAAC ACAGGACTTG 600
CCCACCGTGG GAGAAAGTAA GGCCATAGGT GTCTCAGGAA CCTGCCCAAA CTCGCCTGGC 660
TGCACGGTGA CAATTCAACC AGCTTTCTTA CCCAAGGTCT GTTGGTGACC AGAGAAAACC 720
TTAGATGACC GGCTGCCATG ATGGCCTTAT ATCTGTCCCT TTTCTGCCAG CCTTGAGGTA 780
GAGGGTGCCA GGGAGGAGGA CTCTGGCTCT AGGTGTTAAA GTGAGAGGGA AGTGTGAAGG 840
GTATCTGTAT AGCTAGACAG GGCTCAATGC CAGGCAGAGC TGTCTCCGCC CCTTTGATGT 900
CTATGTCTCT GTCCCTGGAC TGTGGCCAGT AGCCAGTGTG GACTCCAACC TCACCAGCTT 960
TAGGGGTGTT ATCTGCCTGG GAGTCACTGA TCCTTACTCC CTCCTCTGAC AGCCACCTTG 1020
GATGGGGTGA AAGGAAGGAC AGCCTGCCAA GTATGAGATA AAAACGCCTC ATAAACAAGA 1080
AGGGATTTGC AGGCCAGGCA GAGAGCCTTG TGCTGCTTCT GAGTCCCAGG AGCATGGGCG 1140
AGGAGGTGAG GTCAGGCACT CAGCAGCTGC TGGTCCTCTC TGAAATCTTT GGCCAGATTT 1200
ATTGCTACTG CTTGCTAATA AATGGTTATG CATTTGGTTC AAAGGACCAA GTGTGCTTAC 1260
ATGAAAACTG GCTGTGTTCC CTGGCCTCTG TTTCCTTAGC TGGTTGGACT AATTTGATTG 1320
GTTAATAAAT GAGTCCAAGG TGGTTGGGCT AATTTTTATC TTAGATTCTA TGACTCTATA 1380
ACTGCTACTC AAAAAAAGTG TACTTGTTCC TTTAATCTTT AATCTTATTT TTCTTGAGTA 1440
GTAGAATACA CCCAATTTTT TTCAAGGGGT AGAGAATGCA TTTTTTTTTT AACCTTCCAG 1500
TTTGGTCCCT AGAGTAAACA CAGCATTGCT GTAGTAGATG TAGGGTACTG GAGGGAGCAT 1560
GGAACAGGGA ACCAGAAGCC CTGGTTCCTA CCCCAGCTGG GCATCTGGGC CAGTCTCTTG 1620
ATTCCTCTGT GCCTCAGTTA CCAACTATAT AACGGGCATT CTGCCATGAA TACCCTGCGA 1680
TTTGGAAACC TCCTGTGTAC GTGTGCACTT GGGTGCCTGG CATTCATTCC TAATGGCATC 1740
CATTCGTTCA CACATTCATC CAGTACTCAG CAGACTCCTG CCATGGGCCA GGCAACGTCC 1800
CGGGCACTTG GAATATAATG GAGAACAAAG CAGGGTGCCT ACTTCTGTGG TGCTTGGAGT 1860
CTTGAGGGGA AGAGAGACAC GGAATTCGTA ATTACATGGC AGCGTGTGGG TGACGTATTG 1920
CAGAATGAGG GCCTAGTGGA GCTGGGGGAC CGGAAACGAT GTTTAGGCCG AGACCTGGAA 1980
TAGGAGGAGT TGTCGTGGGG ATGATGTAGG AAGAACGAGT GTGAGGAGGA GAGCGAGGGG 2040
AGTTGAGGGG AGGGCTCCAC ACCTTCTAAG GAGTGGGGAG AGATGAGGCC TCCAAGGACA 2100
GAAGGGCCCT GCAGGCCACG CTGAGGAGCT TGGACTTCAT CTTGTGGATG GTGGCAGGCC 2160
CTTGAAGGGT TTTCTAATCC AGGGAGTGGG GTGGCTGGAT CATGGCTTCA GAAGGCTCTC 2220
CCAGGCAGCT GGATGGTGAA GACCAGGTTG GGGAGGTCAC CAGGAGAATG CTGCCCTAAT 2280
CCAGGCAGAG GTGACGGTAG CCTGGGCCAC TTCATCATTA TCACTGAGGC CTCTCGTGGC 2340
TTCCTCAGAC CAGAACGAAG CCCCCTTCTT CAGTGGCTGT GGGCTCACCA AGTGTCTTCT 2400
CCCTCCTCCA 2410
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