| Tag | Content |
|---|
EnhancerAtlas ID | HS076-18476 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr14:93516100-93519250 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr14:93516391-93516407 | TCCCTTTCGAGGAATG | + | 6.03 | | MYCN | MA0104.4 | chr14:93518390-93518402 | GGCCACGTGGTG | + | 6.07 | | MYCN | MA0104.4 | chr14:93518390-93518402 | GGCCACGTGGTG | - | 6.07 | | Sox3 | MA0514.1 | chr14:93516420-93516430 | AAAACAAAGG | - | 6.02 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_04808 | chr14:93515063-93517663 | Brain_Cingulate_Gyrus | | SE_05777 | chr14:93515009-93517419 | Brain_Hippocampus_Middle | | SE_07721 | chr14:93514989-93517678 | Brain_Inferior_Temporal_Lobe | | SE_23185 | chr14:93514643-93517742 | Colon_Crypt_1 | | SE_23185 | chr14:93517909-93519336 | Colon_Crypt_1 | | SE_23918 | chr14:93515917-93517626 | Colon_Crypt_2 | | SE_23918 | chr14:93517982-93518530 | Colon_Crypt_2 | | SE_23918 | chr14:93518686-93519316 | Colon_Crypt_2 | | SE_26366 | chr14:93514828-93517504 | Duodenum_Smooth_Muscle | | SE_26366 | chr14:93517795-93519317 | Duodenum_Smooth_Muscle | | SE_26889 | chr14:93515678-93517389 | Esophagus | | SE_27639 | chr14:93505251-93519390 | Fetal_Intestine | | SE_28556 | chr14:93505100-93524844 | Fetal_Intestine_Large | | SE_34796 | chr14:93514383-93517278 | HeLa | | SE_40660 | chr14:93515296-93517600 | Left_Ventricle | | SE_41563 | chr14:93515396-93517833 | LNCaP | | SE_41563 | chr14:93517947-93518595 | LNCaP | | SE_41563 | chr14:93518658-93519315 | LNCaP | | SE_42451 | chr14:93516011-93517008 | Lung | | SE_48575 | chr14:93515292-93517306 | Right_Atrium | | SE_50538 | chr14:93514668-93519357 | Sigmoid_Colon | | SE_52403 | chr14:93505242-93519331 | Small_Intestine | | SE_65267 | chr14:93514720-93517598 | Pancreatic_islets | | SE_65267 | chr14:93518697-93519283 | Pancreatic_islets | | SE_68696 | chr14:93515420-93520798 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I093038 | chr14 | 93504881 | 93524683 |
|
Enhancer Sequence | TGGGGGGTGG GTAAGGAAAT ATCCAGAGGG AAAAATCAAC AGAACCTGGA AACAGAAAAG 60
ATGTGGATGT GGAGGGACAG AGGCACCGGG CTGGCAGCTG GGGTGGGAGA TGGGGGGAGA 120
CCTTCATGAC CATCTAAGAA AACACAGCAC AAGCAGATTT GGAAGGGACA GAGGGAGTCA 180
AGTTACAAAC ACGGTCCCTC CAGGCAGAGG CACTTGGCAA AGGTTCTAGG CCTGCCATGG 240
GGGTGGGCGC CGACAATCCC TGCTGCTGGG AAGTGCAACT CCTGCTCAGC TTCCCTTTCG 300
AGGAATGGCC TTCCCGGGGC AAAACAAAGG CCAGGGGGCA GCAGGCCGTA GGAAATACTC 360
TCACTGCCTT AAATAGAAGC AAACCATCTG GCCAGTTGGA GAAAGTTTAC ACAAGGAGGA 420
CTGGGTTGCA CTCGGTGCAT TTTAAAGAAA GCCCGGCGGA CACACGGGTT CTCCTGCTGG 480
TGCTGCCAGC CTGGAAAATG ACAGCTGAGA CTCAAGCAGG CAGGATCGGC TGCCTCATCT 540
CCAATTCCCG TGTGTGGGGT GAGAGGAGGT ACTTCCACTC CCCTACCTGG CTGCAAGCCC 600
CCGAATATGT CCTGTCTAGG GAGGCCCTGC TGCCACACAG CAAAAAATAA GTGATTCACT 660
CTTGAGTTCC ACGTGCTCCA AATGGTTCTC CAAGAGCCCC CAAGTGTCAA CTTCTGTCCT 720
ATCCAAGGCA AGAGAGAGGA GCAAGGGCTG ATGGCGGGCA CCCAGGGATC GCAGGTGGCC 780
GAATACTGCA GCTGGCTTTT GAAGGCATCG ATGCACACTT TGAGGGCCTG CCTTGGCTCC 840
TGCACCCCAC CTCAGTTCGT GTTTCCTCCC TTTATTCTCT CCACCCAGAA AGGTGACAAA 900
TCCAAGCCCT GGATGTGAGG GGGGTCCACA AGAGTAATTC TGGAGAGATG GGGTCAGGTG 960
AGGAATGGTT AGAGACCCAG GGAGCCAAGT CACGGGACCT CAGTGACCCC ATGGCTGACC 1020
TACCGAGACC TCCAGTCGCC AGCATCGGGT AGGCCCACAC GTGTGGGGGA GGAAGTGAGT 1080
GTCACTGGCC CATCAGCAAG CAGAGCTGGC AGAGGTACCT GTGCAGGCGA GTCCAATGCC 1140
CAGCTCTTTA ATAAACACGC CTTGCGGTGC TGGAAGAGAC TCAAAGTCCA TCCAAGACAG 1200
ATTCTGTCTT CCCACTAAAC TGGAAGCTCC TTAAGGACCG GGATGTGGCA GTTTTGCTCT 1260
CAGCTATGTG CCCAGTGCTC AGCACAGGGC CCGGCCTGCC TGGGCACTCA GAAGGACACC 1320
TGACGGACAA GGAACCAATC AAACGGTGAT GGCCACACTC CACCCCCAGG ACCTGACAGC 1380
CAACAGTCAT CACGCACCTG GCAGGCCCAC AGCTCTCTGC ACATACACAT GCCTCAATTT 1440
CCCAGGCATG GGGGAGCTGA ATATCCCAGG ATTCTGCCCC AGACACCATG GTTTTCAAAC 1500
TCTCTCTGAC CTCAAATGTC TTTCCTGAAA TGAAATCTAA CATGCAGACC CCAGATCAAA 1560
CACAGATCAA GAGAGAGTGG CTGGGAAAGG TGGCTCACAC CTGTAATCCC TGCACTTTGG 1620
AAGGCCAAGG CGGGCGGATC GCTTGAACTC AGGAGTTTGA GACCAGCCTG GGCAACATAG 1680
TGAAACCCTG TCTCTCCTAA AAATACAAAA ACCAGGCAGG CTTGGTGGCG CATGCCTGTA 1740
ATCCCAGCTA TTCAGGTGGC TGAGGCAGGG GAATCGCTTG AGCCTGGGAG GCGGAGATTG 1800
CAGTGAGTCC AGATCATGCC ACTGCACTCC AGCCTGGGTG ATGGATGAAA CTCTGTCTCA 1860
AAAGAAAAAA AAAAAAAAGA AAGAGCTGCT CAGGTGAAGG GAGTGGTGAG CAACTCATCC 1920
CCCTTGAAAA GCAGGTACCC CTTCAAGGAA CCCCTAGGGG TGCCTCATAG CCAAGCGTGA 1980
AAGCCAATTC AATGAGACCG GAAACCACCC TGTGCCTCCA AATGTCTCAG CATGGGGAAT 2040
GGAAGACAGC AGATTGGGCG GAAGCCCTTC CATTGTAACG CTAACTCACT CCCTAATCCC 2100
TGCCACTGTT ATGGCTATGG GGTACTCACC TCTGCAGTTT TTGGCTAAGA AATGCCAAGA 2160
ATAAGTACCT ATTTCAAGAA CAACTCTGTT GTGAGAAATT CCAGCACATT CCACTCTGAG 2220
GGCACCACCA TCTTCACCCT TTTGTAGCTG GAGCTTGCAC CAGGGGAGCG CCTTCATCTC 2280
TGCCTGGAGG GGCCACGTGG TGGAAGGGGA ATAAGACAGC AGAAAGCACA GAGATTTGGG 2340
TGGCAGAGTC CCCAGGCCAA ATCCCAGCTC TGCCATTTAA AAGATCTGTG ACCATGGGCA 2400
AGTTATTTAA CCTTTCTCAA CTTCAATTTC CATATCCAAA AGGTAGGATA ATTAATTGTC 2460
CCTGCAGCTT GTAGGACTGT CTTTGGGTTT ATATGAGGGA TTTTTTTCAA GTGCTTTATA 2520
AACCACTCCC AAATGTTAGC TCTATTTACA CTGATTTTAT TGCTGGGCTC CTAGGAGGCC 2580
AAAGGCAACA GACTTAGTTT CCACTAAAGG TCTTTTATTA CAACAGACGC CAGGCATCTA 2640
GGGCGGCCTG TTGTCTGAAG AACAGCCTGA TTCTCCCATA ATCCCAAGCT CTCCAAGGTC 2700
TAAGTCTCGA TACCAGGCCC TGGCTGACTC TCTGACCCAG GGAGGCCTGG TCTGGGTTGT 2760
TCTTACCCTG GGGGCCTTAT CTGTCCTTCT GTGAGGGCCA AAGGAACCCC CAGTGGGGTA 2820
GGGGGACGGG AGATCCTTCA GTGGGGCCAG AGACGGCCTG AGAGTGACTC AGTGGGCTGG 2880
AAGTTCGCCC CCAAGCCTCA CCGGCCTTCT GGCTCACTCT ATATTCAATA TAATACCTGC 2940
CCGCACCACC ACCCTCCCTC CAAACCCAGG TCCCCAAGGG GCTGGTGGTA CAGGAAACAG 3000
CCCTACATCT CCCATCCCAG GGTTCAGTCC CTCACTCAGA ACTGGGAAAG GGGCCGGGCA 3060
CAATCTCCCA GATGCCCCAA AGACTTGGAA AGCGCTCTGG TGGCTTTCTG AGCAGGCACA 3120
TCTGGCCCAA CCACACCTTT CGTCACCACT 3150
|
