| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02440 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:154399360-154401670 |
Target genes | | Number: 22 | Name | Ensembl ID |
|
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 | GCCCTCAGTG GACTTCACCT TCTAGGGACT CAGAATTTTT TTTTTTTTTT TGAGACGGAG 60
CTTCGCTCTT TTTGCCCAGG CTGGAGTGCA GTGGCGTGAT CTCGGCTCAC TGCAAGCTCC 120
GCCTCCCTGG TTCAAGCAAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ATTACAGGAG 180
CCTGCCACCA CGCCCAGCAA ATTTTTTGTA TTTTTAGTAG AGACAGGGTT TCACCATGTT 240
GGCCAGGATG GTCTCGATCT CTTGACTTGT GATCCGTCTC GCCTCGGCCT CCCAAAGTGC 300
TGGGATTACA GGTGTGAGGC CCAGCTGGGA CTCAGATTTT GCTGAGGACC AGGACAGTAC 360
TGTGTGCTGT GTCCTGGCCT TGCAGCAGTG AATGTGTCTC CCGTTTCTCA AGGGCAGGTC 420
TCTGGGATGC CTGACTGTGT CTTCCTTGCC AGTGCCTGGC TGCTGCAGCC TCCTCAAATG 480
TTTATCAAAC ACAGGACTTG CCCACCGTGG GAGAAAGTAA GGCCATAGGT GTCTCAGGAA 540
CCTGCCCAAA CTCGCCTGGC TGCACGGTGA CAATTCAACC AGCTTTCTTA CCCAAGGTCT 600
GTTGGTGACC AGAGAAAACC TTAGATGACC GGCTGCCATG ATGGCCTTAT ATCTGTCCCT 660
TTTCTGCCAG CCTTGAGGTA GAGGGTGCCA GGGAGGAGGA CTCTGGCTCT AGGTGTTAAA 720
GTGAGAGGGA AGTGTGAAGG GTATCTGTAT AGCTAGACAG GGCTCAATGC CAGGCAGAGC 780
TGTCTCCGCC CCTTTGATGT CTATGTCTCT GTCCCTGGAC TGTGGCCAGT AGCCAGTGTG 840
GACTCCAACC TCACCAGCTT TAGGGGTGTT ATCTGCCTGG GAGTCACTGA TCCTTACTCC 900
CTCCTCTGAC AGCCACCTTG GATGGGGTGA AAGGAAGGAC AGCCTGCCAA GTATGAGATA 960
AAAACGCCTC ATAAACAAGA AGGGATTTGC AGGCCAGGCA GAGAGCCTTG TGCTGCTTCT 1020
GAGTCCCAGG AGCATGGGCG AGGAGGTGAG GTCAGGCACT CAGCAGCTGC TGGTCCTCTC 1080
TGAAATCTTT GGCCAGATTT ATTGCTACTG CTTGCTAATA AATGGTTATG CATTTGGTTC 1140
AAAGGACCAA GTGTGCTTAC ATGAAAACTG GCTGTGTTCC CTGGCCTCTG TTTCCTTAGC 1200
TGGTTGGACT AATTTGATTG GTTAATAAAT GAGTCCAAGG TGGTTGGGCT AATTTTTATC 1260
TTAGATTCTA TGACTCTATA ACTGCTACTC AAAAAAAGTG TACTTGTTCC TTTAATCTTT 1320
AATCTTATTT TTCTTGAGTA GTAGAATACA CCCAATTTTT TTCAAGGGGT AGAGAATGCA 1380
TTTTTTTTTT AACCTTCCAG TTTGGTCCCT AGAGTAAACA CAGCATTGCT GTAGTAGATG 1440
TAGGGTACTG GAGGGAGCAT GGAACAGGGA ACCAGAAGCC CTGGTTCCTA CCCCAGCTGG 1500
GCATCTGGGC CAGTCTCTTG ATTCCTCTGT GCCTCAGTTA CCAACTATAT AACGGGCATT 1560
CTGCCATGAA TACCCTGCGA TTTGGAAACC TCCTGTGTAC GTGTGCACTT GGGTGCCTGG 1620
CATTCATTCC TAATGGCATC CATTCGTTCA CACATTCATC CAGTACTCAG CAGACTCCTG 1680
CCATGGGCCA GGCAACGTCC CGGGCACTTG GAATATAATG GAGAACAAAG CAGGGTGCCT 1740
ACTTCTGTGG TGCTTGGAGT CTTGAGGGGA AGAGAGACAC GGAATTCGTA ATTACATGGC 1800
AGCGTGTGGG TGACGTATTG CAGAATGAGG GCCTAGTGGA GCTGGGGGAC CGGAAACGAT 1860
GTTTAGGCCG AGACCTGGAA TAGGAGGAGT TGTCGTGGGG ATGATGTAGG AAGAACGAGT 1920
GTGAGGAGGA GAGCGAGGGG AGTTGAGGGG AGGGCTCCAC ACCTTCTAAG GAGTGGGGAG 1980
AGATGAGGCC TCCAAGGACA GAAGGGCCCT GCAGGCCACG CTGAGGAGCT TGGACTTCAT 2040
CTTGTGGATG GTGGCAGGCC CTTGAAGGGT TTTCTAATCC AGGGAGTGGG GTGGCTGGAT 2100
CATGGCTTCA GAAGGCTCTC CCAGGCAGCT GGATGGTGAA GACCAGGTTG GGGAGGTCAC 2160
CAGGAGAATG CTGCCCTAAT CCAGGCAGAG GTGACGGTAG CCTGGGCCAC TTCATCATTA 2220
TCACTGAGGC CTCTCGTGGC TTCCTCAGAC CAGAACGAAG CCCCCTTCTT CAGTGGCTGT 2280
GGGCTCACCA AGTGTCTTCT CCCTCCTCCA 2310
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