| Tag | Content |
|---|
EnhancerAtlas ID | HS196-04021 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr1:212400830-212403540 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:212401139-212401157 | GGAAAGGAGGCAGGGAGG | + | 6.16 | | EWSR1-FLI1 | MA0149.1 | chr1:212403030-212403048 | CCCTCCTCCCTTCCTCTC | - | 6.27 | | EWSR1-FLI1 | MA0149.1 | chr1:212403274-212403292 | GGAGAGAAGGCAGGAAGC | + | 6.39 | | EWSR1-FLI1 | MA0149.1 | chr1:212403008-212403026 | TCTTCCTTGCTTTCTTTC | - | 6.41 | | EWSR1-FLI1 | MA0149.1 | chr1:212403026-212403044 | TTTTCCCTCCTCCCTTCC | - | 6.4 | | EWSR1-FLI1 | MA0149.1 | chr1:212401131-212401149 | GGATGGAAGGAAAGGAGG | + | 6.51 | | EWSR1-FLI1 | MA0149.1 | chr1:212401135-212401153 | GGAAGGAAAGGAGGCAGG | + | 7.18 | | HNF1A | MA0046.2 | chr1:212402044-212402059 | ATTTAATTATTAATC | - | 6.32 | | ZNF263 | MA0528.1 | chr1:212403021-212403042 | CTTTCTTTTCCCTCCTCCCTT | - | 6.09 | | ZNF263 | MA0528.1 | chr1:212403026-212403047 | TTTTCCCTCCTCCCTTCCTCT | - | 6.13 | | ZNF263 | MA0528.1 | chr1:212401156-212401177 | GAAGAAGGAAGAAAAAGGAGA | + | 6.46 | | ZNF263 | MA0528.1 | chr1:212402664-212402685 | CTTTCCTTACCTTCCTCCTTT | - | 6.57 | | ZNF263 | MA0528.1 | chr1:212403018-212403039 | TTTCTTTCTTTTCCCTCCTCC | - | 6.7 | | ZNF263 | MA0528.1 | chr1:212401350-212401371 | CCCTCTTTCCCATCCTCCTTA | - | 6.88 | | ZNF263 | MA0528.1 | chr1:212403029-212403050 | TCCCTCCTCCCTTCCTCTCCC | - | 6 | | ZNF263 | MA0528.1 | chr1:212401347-212401368 | TTTCCCTCTTTCCCATCCTCC | - | 7.01 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_00506 | chr1:212397824-212401716 | Adipose_Nuclei | | SE_31662 | chr1:212400859-212401451 | Gastric | | SE_31662 | chr1:212401468-212402631 | Gastric | | SE_31662 | chr1:212402726-212404120 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr1 | 212403042 | 212403200 | | chr1 | 212403200 | 212403432 | | chr1 | 212401476 | 212401801 | | chr1 | 212401929 | 212402431 | | chr1 | 212403027 | 212403223 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I212227 | chr1 | 212400860 | 212401451 | | GH01I212228 | chr1 | 212401481 | 212403276 |
|
Enhancer Sequence | TGGTTGTCAT GTCTCTATTT TCTTTTATTC TAGAGCGGTA GGTGTGGGGA AATTTTGAGA 60
ACAATATTGT TGCTGAAATC AACTATTGGC TGCCAGGTGG AAATGGCTGC TGCCTCCACT 120
GAGGCACACT GGGCCCCGCC ACATTTATTA GCACAAGCCC TGTGATATGG TTGCATAGCT 180
TGCTTTGCTG AACTTGTTGG TTACTAGCTA CTGCTTAATG ACTGGACATT AGAGACTCTT 240
CTGTTGTTTT TATATTCCCA CCACCTCCAC AGCACCTAAC ACACAGGTGG TCAGTAAAAG 300
TGGATGGAAG GAAAGGAGGC AGGGAGGAAG AAGGAAGAAA AAGGAGAGTG GGAAAGAGGC 360
AGGCACGGGC AGGCCCCCCT GCCTCCATGC CAGGTGGGTA CCTGGAGAGT GACACTGTGC 420
CCTCCTGGGA AGCACCCACA CTCCTTTGAT TGGGGGAAAA CGATTCCATG TGGCATGTGC 480
CTTTTGTCCA AATATGCCTT CTTCCTTCGC ATTCTCCTTT CCCTCTTTCC CATCCTCCTT 540
ACCTGAGCAC TAGTTGGGAT CCCTCAGACC TTCTGCTATC TTTAACTTAG TCTTTCCCTC 600
TCTTCCCATA TACAAGATTA ACATTTGACA TTATTTTAAA AATAATCTGT AATAGATTAT 660
CTTTTCCTAC AATCACACTC ATTTTCCCAA TTCCCTGGGA GATAATTCCC ACAAAATTTG 720
TGGTCAGTAA TTAAATTCCT GACCACAATG AATCATGAGG AATATATACT GTGTTCAGAG 780
GGATGGCGTG GTATCCGTAA GGGAGCATCT GCTGAAGGGA GAGAGAGGAC ACATGGGGGT 840
TAGCCCACAA AGCCAAGGGG AGCTGTCCTC CAAACACAAC CAACAGAGTT TAGCTCAGGC 900
TTCAGGATCA AACTATTGCT TCTATTCTGT GTGGAGAGAA CAATGACTGA ATTGGCTGGA 960
ATAGAACAAA GTTGTTAAAG TGAACTTTCT CCACACCTCA TCTCTAATCC CTAAAATTTT 1020
GACTTAAACA AAATTTTGAG TTAAGCAAAT TTGAATTAAA AATTTTGAGC AGATACAGGG 1080
AATGAATGCA AGAAGCTCTT GATTATCTTC ATGGTGGACT GGCTCATTTT CATTCCGGGC 1140
TGACCTCGTT GATATGTTCT CTACCACTTC TCCTTGCTGA GAAGTAGTTG GCGTCTATTC 1200
AAAGTACACA GGCCATTTAA TTATTAATCG GAGCAAAACA TTATTAGGGA AGTTAAACTG 1260
TTGAGTAGGT GTGTGTGTGT AAACATGTGG ATACTTTCTT GATTATCTAG CTGTTTTGTT 1320
TTGCCTTTTG CCTTTCTGGG TTCCTGCCCC TCTCCATTTG TGGTGATACC TGTAAGGTGA 1380
TTATGCCACT GAATTCCTAA GAGCTTTTTG GTCCCTCTCT CATTCTCCTT GGATGTGTGT 1440
GGAAATGTTT GTCAGCAGGG GCGGACCGGG GAGGGTTCAT GTACACAAGA AGTGACTGAC 1500
CTTGGCCGCT GAGTGGAGTG TGTATTTGTG ACGAGGAAAG GGTTCAGTGT TTGTGTTTGG 1560
TGATGGTTTT ATGTCCTGCT GTCATTAGAG AGGACTTTAT AGGGGTTTCT GATGACCTAG 1620
GGCTCCAGGA ATCATCATGA TTATTTAGAC AATGATTTTA ATGGGCCCAT ATAAACTTAT 1680
TCTGTTTTTA TACTAGTAAC AGAGAAGAAG ATGTTGGAAG ATTAAATATA GAGAAGGATG 1740
GGCTTTAGCG TCACTGTTCA GGGACATTGG GAATTATTCT ACAGAATTCG ATCCAGCCTA 1800
TTCTCATTAT TTCCTTCTTC TTATGACTTT CATTCTTTCC TTACCTTCCT CCTTTTCCCT 1860
TTCTTCTTCT TCTTTTTTTT TTTTTTGAAA CGGAGTCTCT CTCTGCCGCC CAGGCTGGAG 1920
TGCAGTGGTG CAATCTCAGC TCACTGCAAG CTCTGCCTCC CAGGTTCACG GCATTCTCCT 1980
GCCTCAGCCT CCCAACTGGC TGGGACTACA GGCGCCCGCC ACCATGTCCA GCTATTTTTT 2040
TGTATTTTTA GTAGAGACAG GGTTTCACTG CCTTAGCCAG GATGGTCTCG ATCTCCTGAC 2100
CTTGTGATCC ACCTATCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACTGCG 2160
CCCGCCCTCT TCTTTTTTTC TTCCTTGCTT TCTTTCTTTT CCCTCCTCCC TTCCTCTCCC 2220
CACCTTTATT TATTTCTTTC AACATGTACT GCCTGCTTAC TATATATTAG TCACAGTCTA 2280
AATGCTGGAG ATGCAGAGAT GAATAACACA TGGCCCCAGC CCTCCTGGAA CTCAGTTTAG 2340
CGTGGGAGGC AGATGGAGGC ACAGATCATT CCAGTACAGT GGTTAACGAT AGAGATAAGT 2400
ACAGGGTGAG CTCAATGTAG GGGTCCCTAA TCCAGCTTGG CTTGGGAGAG AAGGCAGGAA 2460
GCTTCCTGGA AGAGATGATG GCAGATTGAT TGGGAGTGGC TGAAAAAGGA GCAGGGCTCA 2520
AGGCCTTTAC CTGGCAGGCC AGGTCATTCA CATGGTTTAT GAGCACTGGA TAAAGGGAAT 2580
GGGATGAAGG GCTTTGGGGG TATGGGTCTT CCATGAGATA TGACACCAGA TTTTGATGTC 2640
ACTGCATATG GTTAGGACCA CAGGGGCAGG GCAGAAATGA TGTCTACTAC TGTGGGACAG 2700
TACTAGTGAC 2710
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