| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02439 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:154394480-154397460 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr1:154394661-154394675 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_00437 | chr1:154390273-154397370 | Adipose_Nuclei | | SE_01040 | chr1:154395089-154396159 | Adrenal_Gland | | SE_01040 | chr1:154396167-154397057 | Adrenal_Gland | | SE_06653 | chr1:154394457-154397543 | Brain_Hippocampus_Middle | | SE_09117 | chr1:154396547-154396857 | Brain_Mid_Frontal_Lobe | | SE_09189 | chr1:154388527-154398657 | CD14 | | SE_17632 | chr1:154395162-154397013 | CD4p_CD25-_CD45RAp_Naive | | SE_18405 | chr1:154394565-154397419 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19165 | chr1:154394817-154396790 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_26877 | chr1:154390381-154397107 | Esophagus | | SE_32086 | chr1:154395033-154395588 | Gastric | | SE_32086 | chr1:154396321-154396899 | Gastric | | SE_36673 | chr1:154394402-154396551 | HMEC | | SE_41139 | chr1:154394811-154397130 | Left_Ventricle | | SE_42431 | chr1:154394877-154395745 | Lung | | SE_42431 | chr1:154395793-154397326 | Lung | | SE_44716 | chr1:154394952-154397278 | NHDF-Ad | | SE_47983 | chr1:154396365-154396816 | Pancreas | | SE_48261 | chr1:154388323-154397557 | Psoas_Muscle | | SE_48934 | chr1:154395791-154397087 | Right_Atrium | | SE_50453 | chr1:154394901-154397519 | Sigmoid_Colon | | SE_51380 | chr1:154394475-154397322 | Skeletal_Muscle | | SE_52880 | chr1:154395805-154396974 | Small_Intestine | | SE_54618 | chr1:154390203-154397361 | Stomach_Smooth_Muscle | | SE_62668 | chr1:154357227-154415486 | Tonsil | | SE_64458 | chr1:154393145-154396883 | NHEK | | SE_65390 | chr1:154390491-154396964 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr1 | 154394967 | 154395363 | | chr1 | 154394684 | 154394789 | | chr1 | 154395885 | 154396482 | | chr1 | 154395894 | 154396284 | | chr1 | 154395096 | 154395640 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I154417 | chr1 | 154390221 | 154396888 |
|
Enhancer Sequence | GGTGCAATCT CAGTTCACTG CAATCTCTGC CTCCTGGGTT CAAGTGATTC TCCTGCCTCA 60
GCCTCCTGAG TAGCTGGGAT TACAGGTGTG TGCCACCACG CCCGGCTAAT TTTGTATTTT 120
TAGTATGGGG TTTCTCCATG TTGGTCAGGC TGCTCTCAAA CTCCCGACCT CAGGTGATCT 180
GCCCGCCTCG GCCTCCCACA GTGCTGGGAT TACAGGCGTG AGCCACGGCG CCTGGTGACT 240
CAGTTCTTAA TGCCTTGCAT ATACTGTTCT CTCTTTATGG AATGTAACTC CCTGTGGCTC 300
CACTTATCAA ACCCCCACTC ATTTATCAAG GCCCCAATAA AATCTCTCTT CCCCCTTTAG 360
AATAATTGAT CCCTCTTCTT AGTTCCCTCA GTATGTTGGA GACATTTATA TCAGGTTGGC 420
CTGTATTACA GATAGTTTTA AGTTCTAGGG CTTTGTGGGG TTTAAAGAAG ATTACGATAT 480
GGAAATGATA GGAAGGAGTG CCAGTGCATT GTAGATGCTC AGTAGCTTCA ATATGGAGTT 540
TTTTTTTTCC TGGATTAGGA ACTTCTGAAC TTGCACATCA TGGGTGCACA AAAATTATTG 600
AATTCTTGAA GAAGGGACAG GCATAGGCTT GCAATCCTGG CTCTGAATGC TGAGCAATTG 660
CTCACGGACA AATGCTCCGT TGATTGTGTG CTCTTTGCTA AATTTCAGTG TGTGCACCAG 720
CCACGCCTTC GCCCCCGCGT GCCCCGTCTC CTAGGGCCTA CTATGCAAGG CCTGTGTCAG 780
GCCGGGGTGG GAGCATGAGA ATGACTGGGC ATATCTCCCA GGACCAGGAA GGACTGCTCT 840
CAGGAGCCCC CTCCTCACCT GGTTCCTCAT CGTGTCTCTT CCTTTTGGCC CTTCTCTTTG 900
GTAGGGCCTA CTTAGGGAGG GCCCCAGCAG ATTCCCAGGG AACAGAAAAA CAGACAGATG 960
GGAGGAATCA AGGCTGAGCC CAGGGATGGT GTCTTGTGTC CACCAGGGAA TCAGGCCTAC 1020
AGGGGAGGGC TGGGCTATGG GTGCAGAATT CAGTGACAGT GACAGTGAGA GAACTCAGCA 1080
GTGCAAGGGC AAAGTGGCAC TGTTTGGCCT GAAGGTGCTC GGAAGCTGCT TGTATTGAAA 1140
AATCCACCCT CATCCCCCGA CATCCCTCAG TGCCCACTGC GCTCTGCCGT GCCCTCTCCC 1200
TCCTTCCTAG AAATCCTAAC TCACACAGAC CCAGGCTATG TAGCTTGTTT AATTAAATAT 1260
ATATATATAT ATATATATAT GTATTCATTA TAAGAGCAAT ATAGGCAACT TATAGAAAAT 1320
TCAAAAACTA CAGAAAGACA CAGGGAAGAG AAAGAAATCA CCTCTAACAC CATCATTTGG 1380
AGAGGAGGGC AGAGGTAGGG AGAGGACACT TCTATGAATG TTACTTGTTC TGAGAGTCAC 1440
CCATGAGGCT TCCCCACTGC CACCCAGCTG TCAGGGGTAC TGAGTCAGAG ATTTGGGTCA 1500
GGAGGCAGAG GGCTGAGTGG GTGGGAGGGA AGGGGCGGTG CTGCCCACTC TGACTTTAGC 1560
AAGTATGTTT TCTTATAGTC TTTATGAGTA TTTCTTTGAT CATTCTGCAT ACAGTGCTTT 1620
TAAAAGCGTA GTTAACACAG TGTTGTTCGC AGGTTCTAGA GGAAATATAT TTTGAAGCAG 1680
GGCTGTGACA GGCAATACTT GCCAATGGGT GGTTTATAAT TAATCATTCC CTGTTTTAAA 1740
AAATAGTGAC TCAGTTTTAA AGATTCAGAA AGCCATTACT CAAGTTCCTT GGCAGAGGAA 1800
GTGGCCATTA TGTTGCTCCC TGCAGCTCTG CTTTTGTGGA AGAGGGAAAA AAAAGTATTT 1860
TTATTTGGTA TTTCTCTGAG CTGCTCAGAT ACTTTGGCCA TTGTTAGTGA GTGCAGGAGC 1920
AGAACAGCCC CTGCTATTGT TCAGGCTGGC CGCTAAACAT GGCAAGAGCT TCCCGCTGAA 1980
CTGGGGTAGG GGAAATGACC AGAAAGACAT TTACTGGATT TGGCAAAGGC AGAAGCAGAA 2040
AAGAGAGCTT CCTCTGGCTC CAGGAGTCTA TTTCTTGCCT CAGCGGGCTC CTCTGCCCCC 2100
CAGCCTGGGG CCTGCCCATC ACACAACACG AGAGGGCACC ACTTAGACCC CTTCACCTGC 2160
AAACCGTGCG CCTGGGAGTT TTTGGTGCCG AGACCCTGTC CCTGTGGGCA CCCCTAACAT 2220
GCCCTATATT CAACAAACAT GCATGAAGCA CCTACTAAGT TCTCTGATGA GTGACGACCA 2280
GGAGCTTCCA GTGTTGTCAC CATGGTCGGG GAAGGGACCT TTATATAGTT GAGGACTGTG 2340
CCATGTGAAA AGTGCCAGTG ATTGGATGAG CTGCAGTGGT CCTTGACCCC TACCTTAGAC 2400
CTTCATGCAT CCTGCACTTG TGTCTGTTGC ATGCCATGTG AATTCTGATT TCTGCTAATC 2460
AGCGAATCAG CTGAGGAAGG GATATTGCAA GCATTGCACT GGGAGCAGTT CTCTTTGGGC 2520
ACTGTTTCCA TCTTTGCTCC TGCAAGTTTG TCATTTGTGC AGGAACTTGA AATCCGTGTT 2580
AGGTTTTATC TTGACAGCTG CTTTATCCAG TGGAAAATGG AAAAGTGGAA ATATTGATGC 2640
ACTGATTAGA AGTGTCGTTG CATCTTCCAT ACGTAACCGC ATTCAGGCAC TGATGGACTT 2700
CAAGATGTGG GCTGGATGTG GTAAACTGCT GCCTCCATCA GGTGCTCATT GGAGTTCAAC 2760
GCACTGGACC GTGTGTTCAG TTGTGATGTA GCAGGACAAG CCACAGACAA AACCCCTCAG 2820
ACACCGAGTT AAAGAAGGAA GGGCTTCATT CGGCTGGGAG CTTCAGCAAG ACTCATGCCT 2880
CCAACAACCG AGCTCCCCGA GTGAGCAATT CCTGTCCCTT TTAAGGGCTC ACAACTCCAA 2940
AGGGGTCCGC ATGAGAGGGT TGTGATTGAT TGAGCAAGCA 2980
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