| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03886 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:235146970-235149890 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:235147328-235147348 | CCCCCACACACACCCACGCC | + | 6.07 | | ZNF263 | MA0528.1 | chr1:235147070-235147091 | TTTTCCTCTCTCACCTCCCCC | - | 6.41 | | ZNF263 | MA0528.1 | chr1:235148891-235148912 | GAAGAAGGGCGGGGGAGAGGA | + | 6.65 |
|
| | Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
| SE_02305 | chr1:235147035-235148901 | Astrocytes | | SE_06052 | chr1:235147258-235149727 | Brain_Hippocampus_Middle | | SE_25800 | chr1:235146945-235149402 | Duodenum_Smooth_Muscle | | SE_26806 | chr1:235147079-235148893 | Esophagus | | SE_29689 | chr1:235147728-235149217 | Fetal_Muscle | | SE_31235 | chr1:235146510-235149391 | Fetal_Thymus | | SE_32614 | chr1:235140175-235154143 | GM12878 | | SE_33758 | chr1:235147075-235148879 | HCC1954 | | SE_34767 | chr1:235147005-235148891 | HeLa | | SE_36058 | chr1:235146614-235149471 | HMEC | | SE_36952 | chr1:235146938-235152568 | HSMMtube | | SE_37966 | chr1:235146872-235149155 | HUVEC | | SE_40653 | chr1:235147027-235149414 | Left_Ventricle | | SE_42265 | chr1:235147105-235148992 | Lung | | SE_44202 | chr1:235146927-235148930 | NHDF-Ad | | SE_45558 | chr1:235146593-235149758 | Osteoblasts | | SE_47119 | chr1:235148155-235149767 | Panc1 | | SE_50071 | chr1:235146899-235149198 | Sigmoid_Colon | | SE_51271 | chr1:235147542-235149156 | Skeletal_Muscle | | SE_52352 | chr1:235147001-235149055 | Small_Intestine | | SE_53330 | chr1:235146848-235149167 | Spleen | | SE_56068 | chr1:235146597-235149251 | u87 | | SE_57395 | chr1:235146972-235147669 | VACO_503 | | SE_59274 | chr1:235138265-235187641 | Ly3 | | SE_60969 | chr1:235059965-235155853 | HBL1 | | SE_62329 | chr1:235047040-235185428 | Tonsil | | SE_63542 | chr1:235146861-235147654 | HSMM | | SE_63542 | chr1:235147688-235148831 | HSMM | | SE_65393 | chr1:235146807-235149156 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 235146978 | 235147112 | | chr1 | 235148474 | 235149499 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I235010 | chr1 | 235145789 | 235150146 |
|
Enhancer Sequence | AAAGACTGTG GGTTCCTTGC ATCAAGCCGG GGCTTTTAGT CAACTCTCCC ATGGGGACTC 60
TGTTGGCCCG CTCCACCTCG GGTGTTCCCC CGCCCCTGCC TTTTCCTCTC TCACCTCCCC 120
CATCCACCCC TCTCAGCCTT GCAGTCGACC TGCCTCTCCT CTGGTTGCTC CGTTTGTAGG 180
GAGGGTCTGC TTGAAGGGAG TTCCCATTCT CTCTCACCCA GAGTCAAGGC TCTTGACTCT 240
ATTGTACCTA AAAAGCTCCT GAGGAATTTG ACAAGGCCCC ACCCTCAGAG ATATGGGGTG 300
AAGCCCAGGA ATCTGTATTT TTAACAAGCA TCCCAGGTGA TCCTGATACT TGCACACACC 360
CCCACACACA CCCACGCCGA CTACCCACAC ACTTCCATGG CCCAGAAGTC TGCAGGACCC 420
ACAGCAGGTA TTCGGGACTA TTTGTTCAAT CCACACCTGA GTCGTTGCAC GATTATGCTC 480
AAGTCCCTCG GAACACCTCG CCTGCCATCT GACAGCTTCC CATCCAGAAA CCACACAGTA 540
CAGTAAAAAA CAGAAAAAAG AAAGCCGTTA GACCCCAGTG AATGTTATTT TTAATGAAAG 600
TGGTGCATTT TGACTCACAA TGTTGAAACC AGATTATAAA TGAGTCATCA GTGAATCGAC 660
CACAAAGAGC CTTTGCGGAG GTGATTTACA GGAGAGCTCT GATGTCTGCT GTCCCCTGCA 720
CACGCTTCAC AGAGATGCTG TCAGACGCAG AGCTGGTCTG GGGCATCTGT TGCCGCGTCA 780
GCTCAAAAGG ATGCTGTGTT GTCACCAATG GGATTCCCCA GCCCAGGCGG TGTTGCGGTC 840
CCACCCACAC AAGGAAGGCG GCCATCACTG AATAATGCTT GTGGTTACAT CATCATTGCT 900
GGTTTCCAGG TAGTGACTAG CAGATACTGG AGAGAGACAG GCCATCTGCT CTTCCTGTGC 960
GCCTCAGCTC CTCCCTCATA CCCACATCCT CTCGCCTGGT CTTCTAGAAG CAGCCCCTAT 1020
GCAGACAGAC CAGCAGGACT GAAAGCTGGA CAGACTCGAG CCGGAGAGCC AGGTGGAACA 1080
ACCTGGCCAG AAAGAGTCTG GCCGCAAAGA GTCTGGCCAC AGCCCCACTT TCCTCATCTC 1140
TAAAATGTCC ACATGGCTGC CTGCCCTGCC CGGCTCAAGG GAATGTTGCA AGGCTCTCAT 1200
GGAAACCATG CTTGTGAGGG TTTTGAGGAC TATCATAGCC CGTCCCAAGG TCAGAGGACA 1260
GTAGAAAACA AAAAACTTGC TTTCAGAGGG TGCTTTCACC AGTCAGCAGC CTCTGCCCCG 1320
GGCAAAGCCA GACAACTAAA ACGGAATGAA TCCGCAGAGT AGGGTGGGGA TGAAATTCTC 1380
CACCTCCAAC CCAGAAAGGA AACGCCAATG CTCATGTTTC CCCTTAGAGA AACAGGCAAT 1440
GTTTGAACAG GAACAACGAC GCCAGAGGGT CAATCCACAC ACAGAACACT CCATCTCCAT 1500
GCCGATGGGG GACTGACTGT CCTGCTGCTG AACTGCACCC CTGGGGCTCT CCAGGACACT 1560
CCACTGGTGG CCACACTCAG GAAAATAAAG AAAAACCTTC AAAAGGACCC TTCTGGCCAT 1620
TCAGAGAATG CACAGGCCTG CTAGCTCCTG CTTGCCTGCT CAGAGCTGCC TCCACTGGGG 1680
CAGGAATCTG CAGCCAAGAA AATCCCTGAC AACCCCAGGG ACAGAAGGGT CAGTCTGGGG 1740
GACCATCGAC CAACCCAGCA ACCCAGATTA GACTGCTCCA CCAGGAACTC TGTGTCCAGA 1800
GAGCAGGATC TGCCACAAGC AAAACTAGGC CTCATTTACT ATTCCACAAT AGCAACTAGA 1860
AAGCATGTGA CCCAGAAAAC CTTCAAAGAA GGCCAGAAAT TCATTAAATC TGAAAAGAAG 1920
GGAAGAAGGG CGGGGGAGAG GAAAACACTG CTTAGCAAAG CCAACTGAAT CCCTCTTCCA 1980
TACATCACAG ATGCAGGACC AGTCTCAGCA TTCAAGAGGA AGAGAAAAAT GAAAACAAAA 2040
ACCAATCTGG AGTTGAATGT CAGCCTTCCC CTCACTGGTT CTGGGTCCTT TGGAAGGCCA 2100
TATTGTCCCC GGACCTCTCT TGCTTCAGTG GCCTTCCTGC CAGGATTGCC ATAAGGATTA 2160
AATGGACTCA TATATGTGTT GTACCTATAC AGTACCTGCA ACACAGTAAA TATCCAATAA 2220
ATGTTGGTTT CTTGCTACAA GAAATTGTAA AATATGGGCA CAAATTCCTC CTACTTTGTT 2280
AAGCACATCC CTTGGCAATG ACTTAGCTGC TACTCCCATC AAGAGTTGTG GTCTATGTCC 2340
CTACCCCTTG AATCTGGGCT AGCCTGGGAC TTGCCTCAAC CAGTAGAATT TAACAAAAGT 2400
TACAGTGTGT GACTTCCAAG GCTAGCCCTT GCCGCTTCCA CTTTTGCCCT CTTGGAATGT 2460
GGCCCAGAGA CAACCATCTA AGGAAGCTGA TCTAGGCCAC TGGAAGAGGG GTGGGCAGAT 2520
GGAGAAGTGA TGTCCCCCAA CCAGCTGCCA GTCACATGAG AGAGGCCATC TCAGATCTTC 2580
CGGCCCAGCT GAGCATTCAA CTAAATGCAG TCACATTAGT GAGCCCAAGC AAAACCGGCA 2640
GAACTGTCCA GACAACTCAT AAAATCAGGA AAACAATCAA TTCTTGTTTT TTTTGTTTGT 2700
GTTTTGAGAT GGAGTCTCTG TTGTAAGGCT GGAGTACAGT GGTGCTGTCT TGGCTCACTG 2760
CAACCTCTGC CTCCTGGGCT CAAGCGATTC TCCTGCCTCA GCCTCCTGAG TAGCTGGGAC 2820
TACAGGTGCC CGCCACCACG CTCGGCTAAT TTTTTATATT TTTAGTAGAG ATGGGGTTTC 2880
ATCATGTTGG CAAGTATGGT CTCAATCGCT TGACCTCGTG 2920
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