| Tag | Content |
|---|
EnhancerAtlas ID | HS046-00326 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr1:16514150-16517050 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:16514416-16514435 | TGCCGCCCTCTGGTGGCTG | - | 8.01 | | FOSL1 | MA0477.1 | chr1:16514795-16514806 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr1:16514795-16514806 | GGTGACTCATG | + | 6.02 | | KLF4 | MA0039.3 | chr1:16515443-16515454 | CCACACCCTGC | + | 6.62 | | TP63 | MA0525.2 | chr1:16514924-16514942 | AGCATGTTGGCACATGCC | + | 6.01 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_23091 | chr1:16514094-16514451 | Colon_Crypt_1 | | SE_23091 | chr1:16515057-16516232 | Colon_Crypt_1 | | SE_23751 | chr1:16514119-16514463 | Colon_Crypt_2 | | SE_23751 | chr1:16515130-16516087 | Colon_Crypt_2 | | SE_24743 | chr1:16514042-16514476 | Colon_Crypt_3 | | SE_24743 | chr1:16515648-16516115 | Colon_Crypt_3 | | SE_24743 | chr1:16516242-16516615 | Colon_Crypt_3 | | SE_26540 | chr1:16513910-16517815 | Esophagus | | SE_28102 | chr1:16515172-16516184 | Fetal_Intestine | | SE_29455 | chr1:16515096-16516063 | Fetal_Intestine_Large | | SE_31527 | chr1:16515204-16516074 | Gastric | | SE_34268 | chr1:16514127-16516193 | HCT-116 | | SE_34628 | chr1:16513819-16517068 | HeLa | | SE_36144 | chr1:16514154-16516161 | HMEC | | SE_47150 | chr1:16512880-16515228 | Panc1 | | SE_50427 | chr1:16514084-16516281 | Sigmoid_Colon | | SE_52536 | chr1:16514970-16516287 | Small_Intestine | | SE_56795 | chr1:16513668-16515000 | VACO_400 | | SE_64726 | chr1:16514111-16515805 | NHEK | | SE_65472 | chr1:16514077-16514502 | Pancreatic_islets | | SE_65472 | chr1:16516042-16517079 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I016189 | chr1 | 16516243 | 16516615 | | GH01I016187 | chr1 | 16513841 | 16516098 |
|
Enhancer Sequence | ACATCATAGG ACCAAGGGGG TGGTCTCTGG AGCCTCTGAG CATGTTTCAG ACTTAGGAAC 60
CCTCACAGCT GAGGCCAGGA CTGGCCATGT GCTCCTGTCT CCAGGGCTCT ATGCCCTCCC 120
TTCCCTCTAC CCAGCCCACT GCCCCTGCCC CTACTCCCTA CCCCTGCCCC ACAGACACAG 180
CCAAGCCTCA GGAGGACTCA ACCCACAGGA ATGTGGGCAA TGAGCAGGCT GCGCTCGGAG 240
GACCCCGCTA TCCCAGCCCT GGGCTCTGCC GCCCTCTGGT GGCTGGGCTG GGAAGGATGC 300
TGCTCCCATT ACTGCCGTTG TAGAACCGCA ATTGCCCTAA AAAAATAAAA TGCTGTTGCT 360
GCTACTCATG ATGATGACGA TGATGGCGAT GACGATGATG ATGATATTCA TTGCTTTATG 420
GTTTGCCAAG TACCTTCTCC GTCAATCATA GGCTGCACCA AACAGAGTGC AGGGTTCTGG 480
ACTGAAATCA GATGGGAATG TAAGTCCCTA GTCAAGTTCC AACTGATTAT GTGACCTTGG 540
GCAAGTCATG TCACTTCCTT GAGCCTCAGA CTCCTCATCT GTGGAACGGG GTGACAAAAA 600
TAGGGTTGTT ATAAGGATTA AAAGACCTAA CACCTGGCCG GGCGTGGTGA CTCATGCCTG 660
TAACACCAGC ACTTTGGGAG GCCGAGGTAG GAGGACTGCT TGAGCTCAGG AGTTTGAGAC 720
CAGCCCGGGC AAATGGTGAA ACCCCACCTC CACTAAAAAT ACAAAAAATA GCCAAGCATG 780
TTGGCACATG CCTGTAATTC CAGCTACTCA GGAGGCCGAG ACTTGAGAAT CGCTTGAACC 840
CAGGAGGTGG AGATTGCAGT GAGCCTAGAT CACACCACTG CACTCCAGCC TGGGCGACAG 900
AATGAGACTC TGTCAAAAAC AAAACAAACA ACAACAACAA CAACAAACCA TCTATTGAAC 960
TAAATTGGCC TCCAAAATAT ACCCTTCTGG AATTTAGGTG GCTATTAAAA GACCTAACAC 1020
CTGGCACTTG GGTTGGAGAG AATAACATGG CTGTCGTTAT ATACTAATCC TTGGCCAGTC 1080
TGTCCTGGGA GATCAACTCC CCTTTGCATA GGGCTTTTTC GAAGTCCTTT TCCAAGGCAT 1140
CACCTTCTTG TAGCTGCATT ATCATGCCCG TTTACCAGAT GAGGAAACTG AGGCTCAGAG 1200
AGGGGAAGCA GCTTGCCTAG AGCATCGTGG CTTATAAGTT AAAGCAAGAC TCAAGCCAGG 1260
TCCACCTGCC TCCAAACCCG GTGCTGGACT TTCCCACACC CTGCTTTGGA AACTCTAAGG 1320
AACCTTCCAA TCCCCCAAAT CCTATTGCCT CATTTAAGTA AAGCAGGCCT GGTTTCTGCC 1380
TCCTTCAGTG CCCCTCTTCT CCTCCCACAC CCTTCCAGCA GCCGAAACGC TAGACCCAAT 1440
AGCTTACCCC TTCCTCCTTC CTGACCAGCT CCCAACCCTC AGGGCAGCTC ATGAGCCAAG 1500
AGCTTGAGAG TGGCTTCCAA AGGTCATCCT CTCCACCCCG CTGTGCCCCA CCCAAGCAGA 1560
TGACTGTTCA TCCTGTTCTT CACGCTGCTC AGGGGAAGAA ATTCCCCAGC TTCACTCCCT 1620
CCACTCGCCC AGGTGTCTGA GACAGTTCCC ACAGTTGGCA AACTCTGCCT TAAGTCCCAC 1680
CAGAGTCCCT CCTGCTACAA CGTCAGCCCA TTTATTTTAG TTCTTTCTCC CAGTAGCATC 1740
AGAAATACAA TCTGGGGGGA GACAAACGCC GGGAGAGTGG GATCCTGGGA AGGGGAAGGC 1800
ACACTTGGGG ACAGGAAGTG AGAGCAAACC CAGGTTCAAA TCCCGGTCAG GGTGACAAGA 1860
GTGGCCAAGC GAGGCCAGGC GCAGTGGTTC ACACCTGTAA TCTTAGCACT CTGGGAGGCT 1920
GAGGGGGGCA GATCACTTGA GGTCAGAAGT TCGAGACCAG CCTGACCAAC ATGGTGAAAC 1980
TCCGTGTCTA CTAAAAATAT AAAACTTAGC TGGGCGCTGT GGTGGGCGCC TGTAATCCCA 2040
GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAACCCA GGAGGCAGAG GTTGCAGTGA 2100
CCCAGAATGG TGCCACTGCA CTCTAGTCTG GGCGACAGAG TGAGACTTCA TCTAAAAAAA 2160
AAAAAAAAAA GAGCGGCCCA GTGGGTCTCC TGGTGTCCAG GGCAGTCTCA GCCCAGATGG 2220
GGCAGCCCCG CCCACAGCCC GAGGGCATCC AGACCCTCCA CCCCACCATA CTGGCACCAA 2280
GTAGCTCAAA TGAGGGAAGA GAGCTGGGGT GGGACTTGGA AGCAGAGCGG GTCTGAGGGG 2340
CAATTATGAG CTCGGGCTCA GGGTTCATGC AGAGCCGGGC TCAGACCCAG CAACAAATAT 2400
TCACTGAGCT GCTCCTGGGT TCCAGGCATG GCAGTTGGCA ATGAGGCCAC AGCACTGGGA 2460
AGACAGCCAG AGGCCCTTTC TTCATGGATT TCACGGTCCA GTGGGGGAGA CAACAGAAAA 2520
CAGGTCACCA CATGGATCAA CAAGGAATCC CAGAGTGGCC ACTCGGCTCT GCACTGTCCC 2580
CCTCCTGTCA CCTCCATTTC AGCTCTCAGG ATGCAGCTTC AGTGGCACCA CCTCCAGGAA 2640
GCCCACCCTG ACTGCCAGTG AGGACAGGCT GCTCCCTTAT TTGTGCCCCC ACAGCCCCAC 2700
AGTTTGCACT GTGTAAGCTT TCAGCTGAAA TTTAACTCCC ATGCAGAAAA GCACACAGAT 2760
CTTAGGCGCC CAGCCTGATG GACTGGTCCC AAAGTGCACA GCCCTGTGGA AGCAACATCA 2820
GCAGTCCCTC CCTAAGCAGT CACTACTTCA GCTGCAGGCG CTCCCCACCC TGACCTCGAT 2880
CCATCAATTA GTCTGCCTGG 2900
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