| Tag | Content |
|---|
EnhancerAtlas ID | HS104-05102 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:204056380-204058980 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr1:204057583-204057596 | GGCATTTGCATAT | + | 6.3 | | Pou2f3 | MA0627.1 | chr1:204057582-204057598 | TGGCATTTGCATATAA | - | 6.44 | | SPDEF | MA0686.1 | chr1:204058253-204058264 | TACATCCGGGT | - | 6.62 | | ZNF263 | MA0528.1 | chr1:204057285-204057306 | CCCTCATTTACCTTCTCCTCC | - | 6.47 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_01182 | chr1:204056274-204058246 | Adrenal_Gland | | SE_01182 | chr1:204058247-204059454 | Adrenal_Gland | | SE_03017 | chr1:204056278-204058243 | Bladder | | SE_03017 | chr1:204058249-204059534 | Bladder | | SE_04661 | chr1:204056379-204058327 | Brain_Anterior_Caudate | | SE_04661 | chr1:204058370-204059675 | Brain_Anterior_Caudate | | SE_06365 | chr1:204056169-204060053 | Brain_Hippocampus_Middle | | SE_24644 | chr1:204057659-204057977 | Colon_Crypt_2 | | SE_24644 | chr1:204058329-204058842 | Colon_Crypt_2 | | SE_31799 | chr1:204056312-204059529 | Gastric | | SE_41791 | chr1:204056249-204059508 | LNCaP | | SE_42361 | chr1:204054906-204059621 | Lung | | SE_47675 | chr1:204057012-204057426 | Pancreas | | SE_47675 | chr1:204057647-204058068 | Pancreas | | SE_47675 | chr1:204058262-204059202 | Pancreas | | SE_49400 | chr1:204056234-204059271 | Right_Atrium | | SE_50648 | chr1:204056148-204059540 | Sigmoid_Colon | | SE_53078 | chr1:204056234-204059443 | Small_Intestine | | SE_54451 | chr1:204056226-204059533 | Spleen | | SE_65332 | chr1:204054712-204059717 | Pancreatic_islets | | SE_68685 | chr1:204056205-204059260 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 204057041 | 204058591 | | chr1 | 204058173 | 204058362 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I204087 | chr1 | 204056343 | 204060013 |
|
Enhancer Sequence | CAAAAGGGCC AGGCTGCCCA TCACCTGGGT AGATAAGTCA GGCTGGGAGG CCTAGGACTG 60
CTCGCCTTAT ACAGAGGGGT CAGGTGCCTG CCTTCCCAGG GGCACCAGCT GGACCCTGCT 120
GACTCCATGG TGGCTGCAGC TATCTGTTCC AGGACCTTCC TGTAGCTTCC CAGGGCCTGC 180
TCCCTGTGCA TGAGGCAGTA GGCCCCCCTG TCCCACCTTT TCTTATGGGA GCACCCTGAC 240
ATCTCCCCTT TCTGTCTGTG CTGGTGTTTC CGGGAGGTGC TGGGACCACC AGTGCTAAGG 300
CCCTGGTCTA GCTTCTACTG CTAATGGCTT GTATGCCCTC AGGGCTGTCA CTTAGCCACT 360
TGGAGCCTTA CTTCCTCCAT CTGCAACTTG GGAAGGAGCA TTTTGAGTTC TCTTGCTATA 420
AAGTAAGAAT TCTGGTTTGC TGGAAATAGA GTTAGATGAG GATGATGACA ACCACACTGG 480
CAGTTTTTGC TGCAGTTTCA AAGCCCGGAT GTGGAGTCAG ACACTTTGCC ACAGCCCCGC 540
ACAGGATGCT TCTGTGAGGC TTGTCTCGGG TACCTCATAA AACCTTCTAG TTTGGAAGGG 600
CAGGGAGCAT CTACTCCTCA GATTTGGCAG ATGAGGATAT TGGAAATTGT CTAGGTAGTG 660
GGGCTTCCAG AGTCCCACCT GGCTGTGGAT CTGCAGGGAT GAGGCTGGTC TATGCGGTAT 720
GTCTGACTCT GTTCAGAACA AGTGACAGCC CACACTGGGA TCTTGCTTTA GAGTCCCTTG 780
GCCTCCTGCC CTGGCATCTT GCCATTGGTT TTGGGGAAAT GGTGATGGGA AGGGCCCATT 840
GGGTCTCCAG ACAGTCACAG GGAACCATCC TGAGACTGGA TCTGGAAGGA TGTGTGCTTG 900
TAGGGCCCTC ATTTACCTTC TCCTCCCTCA CTTCCCACCT TGGCTGTGGA CGTAGCCCTG 960
TTTTCTCTTC CCCTGTGGTC ATGTTTCTCA GATAGCCACA AAGTGGGCTG AGACCAAGGA 1020
GAGGCATTGG TGCAAAGGGG ATGCTGGTCG ATTCGGCTGG GGACACTACT CTGGGTTCTC 1080
CTAGCCAGGT GGTCAGATGA CTCCCTACGT AGCCTTGGAA ACTGCCCAAA TAAGAAAGAG 1140
AGCGAGGCAG AAAGAGCAGC AGGGACACTC GGATTTTTCC AGGGGCTTTG TCCATATTTA 1200
CATGGCATTT GCATATAACC AGTACACTAA ACATAATTTT ATAATCTATC CCCAGGCACA 1260
TTCAGATTTG CCTTTTACTC TTGTTCTTTC CAGAGATGGC TGGTTCTGCC TTTTTGCACC 1320
TGTCTGTGCC TTCTCACTCC TGTCCCGTTA CCCCCACTCC CAGACTGGGG GTAGGTGACT 1380
GGGAACAGAG TCAGTGTGGG GTAGGGGTCA TTCCTGCTGT TGAACTGATC TGATAAGATG 1440
AGATCAGACC TGACCTCTCT GGGCTTAGCA CAGACGGCTG GATGCACAGG CCCAGCCTCC 1500
CCTCTGCATC CCACCCCAGC GGCCACCACC TCGCCTCGTC AGGGATCAGG ACACCATGCC 1560
TGGCACTCAG CAGGTACCCA TTAAATGTGA AGTGAAAGCT CAATTAGAGT TCGGACAAAT 1620
ACATACTGTG CAGGCTCCTC GGGACCTGGC TTTTGAGCTC ATGAAGGGAG ATGCTGGTGG 1680
GTTGAGGGGA GCCTCCAGTG GTCCAGAGGG TGGGAGGAAT CAATTTCCCT CTCAGCGATT 1740
GTGACCAGGG AGGCATTTCT TTCTCTGCTT GGCCTTGCAG GAAACAGTGT TGAGAATGAG 1800
AGGAGCAGAA AGGAAGAGCT AGGCCTTGTA TTAATTTGTT TTTCAGATTG AGTCTCTGTT 1860
ACTAGCAATT TATTACATCC GGGTCTCCAG CCAAGCACAT TCTGTTCTCC AGTGTTGGGG 1920
GAAGATGCAT GGGGGGGTGG GGAAGAGGCT GGACAGGAAA GAGGAGCAGA TCAACAATTT 1980
TATGACTGAG TGTGTGGTGT CTTGGCGTGC GCTAGAGGAC GGTTTTAGCA CAGGGCATTT 2040
TGAGCCCAGC CCCGTGTGGG GAGGCACTCC TCTGGACAGC ATGGCATTCC CATGCGAGCC 2100
CAGACAGCCC TGGGGAGCAG GATGAATGGG CTTCCCTCCC ACTCTCATGC CCGCCGGCCT 2160
CAGGGTCCAG ATTTCTCTCT GTGAAATGAG GTCAGGACAG TGATGCCTGG AACAAAATCA 2220
TAGTTTCTTG AGGCAGCGGG GCCTGGGGAG ATCCCTCCGA GGAACAGGGG AGCAGCTGTG 2280
TGAGGGGACC CCGGAAGAGG GGTAGCAGGC AAGGCGGCCA CCCTGTGGAA AGAATGGTGC 2340
ACAAGCAAAA CAACCCCCTC TCTGCAAAAG TGCTGAGCTG GTGGAATTTC ACTTGGCGGC 2400
TGTGAGATCA GGGCAGTAGA TAGAGCCCTG CGGGCACCAG GGCTGTGTGG GTGCAGGGGG 2460
TCCCGGAAGA GAGGGCAGGG GCAGCACCTG TGGCACCCTC TCCCCTGAGC TGGCCTCCAC 2520
ATTGCCCAGG GCTCATCACT GGTCCCCATT CCTGGAGGTG CGTCCCTTAT CTCTATCCAC 2580
CTGTCACGTA AGTTGGTCTC 2600
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