| Tag | Content |
|---|
EnhancerAtlas ID | HS174-00331 |
Organism | Homo sapiens |
Tissue/cell | SK-MEL-5 |
Coordinate | chr1:154394630-154397190 |
SNPs | | Number: 1 | 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: 28 | 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 | chr1:154395043-154395299 | Brain_Mid_Frontal_Lobe | | 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 | TGCTCTCAAA CTCCCGACCT CAGGTGATCT GCCCGCCTCG GCCTCCCACA GTGCTGGGAT 60
TACAGGCGTG AGCCACGGCG CCTGGTGACT CAGTTCTTAA TGCCTTGCAT ATACTGTTCT 120
CTCTTTATGG AATGTAACTC CCTGTGGCTC CACTTATCAA ACCCCCACTC ATTTATCAAG 180
GCCCCAATAA AATCTCTCTT CCCCCTTTAG AATAATTGAT CCCTCTTCTT AGTTCCCTCA 240
GTATGTTGGA GACATTTATA TCAGGTTGGC CTGTATTACA GATAGTTTTA AGTTCTAGGG 300
CTTTGTGGGG TTTAAAGAAG ATTACGATAT GGAAATGATA GGAAGGAGTG CCAGTGCATT 360
GTAGATGCTC AGTAGCTTCA ATATGGAGTT TTTTTTTTCC TGGATTAGGA ACTTCTGAAC 420
TTGCACATCA TGGGTGCACA AAAATTATTG AATTCTTGAA GAAGGGACAG GCATAGGCTT 480
GCAATCCTGG CTCTGAATGC TGAGCAATTG CTCACGGACA AATGCTCCGT TGATTGTGTG 540
CTCTTTGCTA AATTTCAGTG TGTGCACCAG CCACGCCTTC GCCCCCGCGT GCCCCGTCTC 600
CTAGGGCCTA CTATGCAAGG CCTGTGTCAG GCCGGGGTGG GAGCATGAGA ATGACTGGGC 660
ATATCTCCCA GGACCAGGAA GGACTGCTCT CAGGAGCCCC CTCCTCACCT GGTTCCTCAT 720
CGTGTCTCTT CCTTTTGGCC CTTCTCTTTG GTAGGGCCTA CTTAGGGAGG GCCCCAGCAG 780
ATTCCCAGGG AACAGAAAAA CAGACAGATG GGAGGAATCA AGGCTGAGCC CAGGGATGGT 840
GTCTTGTGTC CACCAGGGAA TCAGGCCTAC AGGGGAGGGC TGGGCTATGG GTGCAGAATT 900
CAGTGACAGT GACAGTGAGA GAACTCAGCA GTGCAAGGGC AAAGTGGCAC TGTTTGGCCT 960
GAAGGTGCTC GGAAGCTGCT TGTATTGAAA AATCCACCCT CATCCCCCGA CATCCCTCAG 1020
TGCCCACTGC GCTCTGCCGT GCCCTCTCCC TCCTTCCTAG AAATCCTAAC TCACACAGAC 1080
CCAGGCTATG TAGCTTGTTT AATTAAATAT ATATATATAT ATATATATAT GTATTCATTA 1140
TAAGAGCAAT ATAGGCAACT TATAGAAAAT TCAAAAACTA CAGAAAGACA CAGGGAAGAG 1200
AAAGAAATCA CCTCTAACAC CATCATTTGG AGAGGAGGGC AGAGGTAGGG AGAGGACACT 1260
TCTATGAATG TTACTTGTTC TGAGAGTCAC CCATGAGGCT TCCCCACTGC CACCCAGCTG 1320
TCAGGGGTAC TGAGTCAGAG ATTTGGGTCA GGAGGCAGAG GGCTGAGTGG GTGGGAGGGA 1380
AGGGGCGGTG CTGCCCACTC TGACTTTAGC AAGTATGTTT TCTTATAGTC TTTATGAGTA 1440
TTTCTTTGAT CATTCTGCAT ACAGTGCTTT TAAAAGCGTA GTTAACACAG TGTTGTTCGC 1500
AGGTTCTAGA GGAAATATAT TTTGAAGCAG GGCTGTGACA GGCAATACTT GCCAATGGGT 1560
GGTTTATAAT TAATCATTCC CTGTTTTAAA AAATAGTGAC TCAGTTTTAA AGATTCAGAA 1620
AGCCATTACT CAAGTTCCTT GGCAGAGGAA GTGGCCATTA TGTTGCTCCC TGCAGCTCTG 1680
CTTTTGTGGA AGAGGGAAAA AAAAGTATTT TTATTTGGTA TTTCTCTGAG CTGCTCAGAT 1740
ACTTTGGCCA TTGTTAGTGA GTGCAGGAGC AGAACAGCCC CTGCTATTGT TCAGGCTGGC 1800
CGCTAAACAT GGCAAGAGCT TCCCGCTGAA CTGGGGTAGG GGAAATGACC AGAAAGACAT 1860
TTACTGGATT TGGCAAAGGC AGAAGCAGAA AAGAGAGCTT CCTCTGGCTC CAGGAGTCTA 1920
TTTCTTGCCT CAGCGGGCTC CTCTGCCCCC CAGCCTGGGG CCTGCCCATC ACACAACACG 1980
AGAGGGCACC ACTTAGACCC CTTCACCTGC AAACCGTGCG CCTGGGAGTT TTTGGTGCCG 2040
AGACCCTGTC CCTGTGGGCA CCCCTAACAT GCCCTATATT CAACAAACAT GCATGAAGCA 2100
CCTACTAAGT TCTCTGATGA GTGACGACCA GGAGCTTCCA GTGTTGTCAC CATGGTCGGG 2160
GAAGGGACCT TTATATAGTT GAGGACTGTG CCATGTGAAA AGTGCCAGTG ATTGGATGAG 2220
CTGCAGTGGT CCTTGACCCC TACCTTAGAC CTTCATGCAT CCTGCACTTG TGTCTGTTGC 2280
ATGCCATGTG AATTCTGATT TCTGCTAATC AGCGAATCAG CTGAGGAAGG GATATTGCAA 2340
GCATTGCACT GGGAGCAGTT CTCTTTGGGC ACTGTTTCCA TCTTTGCTCC TGCAAGTTTG 2400
TCATTTGTGC AGGAACTTGA AATCCGTGTT AGGTTTTATC TTGACAGCTG CTTTATCCAG 2460
TGGAAAATGG AAAAGTGGAA ATATTGATGC ACTGATTAGA AGTGTCGTTG CATCTTCCAT 2520
ACGTAACCGC ATTCAGGCAC TGATGGACTT CAAGATGTGG 2560
|
