| Tag | Content |
|---|
EnhancerAtlas ID | HS095-09199 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr14:69148730-69150800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr14:69149432-69149442 | GACATATGTT | - | 6.02 | | Stat6 | MA0520.1 | chr14:69149123-69149138 | AGTTCTCTGGAAAGC | - | 6.37 | | ZNF263 | MA0528.1 | chr14:69149384-69149405 | CCATCCTGCTCCCCTTCCCCC | - | 6.03 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_03035 | chr14:69149829-69150429 | Bladder | | SE_09837 | chr14:69145943-69153774 | CD14 | | SE_10804 | chr14:69147805-69153516 | CD19_Primary | | SE_11797 | chr14:69147184-69154238 | CD20 | | SE_25846 | chr14:69147216-69151396 | Duodenum_Smooth_Muscle | | SE_26618 | chr14:69147082-69150870 | Esophagus | | SE_27779 | chr14:69147782-69150672 | Fetal_Intestine | | SE_28733 | chr14:69142983-69154144 | Fetal_Intestine_Large | | SE_29577 | chr14:69146058-69153767 | Fetal_Muscle | | SE_31476 | chr14:69149177-69149668 | Gastric | | SE_31476 | chr14:69149776-69150715 | Gastric | | SE_36049 | chr14:69148571-69151003 | HMEC | | SE_36916 | chr14:69146511-69158224 | HSMMtube | | SE_40886 | chr14:69147194-69149654 | Left_Ventricle | | SE_40886 | chr14:69149746-69152857 | Left_Ventricle | | SE_42158 | chr14:69147179-69151806 | Lung | | SE_44336 | chr14:69146331-69154085 | NHDF-Ad | | SE_46756 | chr14:69149870-69150688 | Ovary | | SE_48603 | chr14:69147190-69151762 | Right_Atrium | | SE_50095 | chr14:69147189-69153363 | Sigmoid_Colon | | SE_51137 | chr14:69146762-69151267 | Skeletal_Muscle | | SE_51770 | chr14:69147182-69154099 | Skeletal_Muscle_Myoblast | | SE_52662 | chr14:69147197-69153302 | Small_Intestine | | SE_54587 | chr14:69148740-69150722 | Stomach_Smooth_Muscle | | SE_55866 | chr14:69148008-69153685 | u87 | | SE_60240 | chr14:69134391-69156849 | Ly4 | | SE_62911 | chr14:69129549-69162790 | Tonsil | | SE_63560 | chr14:69147182-69157806 | HSMM | | SE_65119 | chr14:69148699-69149696 | NHEK | | SE_65119 | chr14:69149700-69150601 | NHEK | | SE_67722 | chr14:69148008-69153685 | u87 |
|
| | 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 |
| GH14I068679 | chr14 | 69145901 | 69157990 |
|
Enhancer Sequence | TCCATGTAAC CAAAAACCAC TCGTACCCCC AAAAATATTA ACATTAAAAA AAAGAATTCC 60
CACCGTGCCT TAAACTTATG TCATCTCACT TTTTTTTTGT CAGCAGCCTA GAGGGAAGGG 120
GACACAATCC CAATTTTAAC ACCAAAGCAA CTGAGACCTA CAGATATTAA ATTACTTGCT 180
CCAGATTACA ACTGAGACTC AAACCCATCG CCTGGCCACA AGTCTGGTGC CCTATCTACA 240
CCAATCTGTC TCCGGTAAAC CTAACTAGCT AGTCAACTTT TCCCATCCAT AGGCCAGACA 300
CCTTTTGAAA TAACAAACCA TCTGATCTCT AGAAAAACTG AAAGGCCAGT TCCAGTTGTC 360
AGACACACCA AGCTCGAGAG AGTCTCTCCC AAAAGTTCTC TGGAAAGCCC AGGGATTCCG 420
AATTCCAAAG CCAGCCAAAT TTGAATTTCC TCTATAAAGA GATAGTCCCT CCTGGTTTAG 480
AACATAACCT TCCTCATTAG GCTGGTTCCA TGTTTTGTAA TAACTTTTGC TTACACCACA 540
AAATTGTCAT AGATTACGAA AACACAAAGG CCTTGGAAAA AAGGCCCAGA GCCCCCTGGA 600
AGTCATTATT TCTTCCTTTA GCAATTGCTG AGTTAAGCAC CATAAATATG GTTCCCATCC 660
TGCTCCCCTT CCCCCGCCCT CCCCGCCCCC CACGATCAGC TGGACATATG TTAGGAAGAA 720
AGCAGGGACG TGGGGGTGGA AGAAGATTCG CATGTCGTGA ATCTTGAGCA CTGAAAAGAA 780
AAAGTGGGGA GAGGGCGGGG AGTTTGCAGC CCTGGAAATG GAATCTCTGA AGGATTTATT 840
GCCTTTGAGT ATCTCACAAG GCTTTTTTTT TTTTAATAAA AATCTGTAGC TTATGGCTTT 900
TTTTTTTTTT TTTTTTTGTA TAGGGCAGTA AACAAGAGCT CTGAAAGGGG AAGGAAGCCA 960
GGAGAAAGCC AGCTCCATTA GTCACGCAGC AGCATATCCT GTCACAAAGG ACCCCAGTTG 1020
AGTAATCGCC CAAAATATGC CTGTTATTTT TTTCTGTCAG AAAAAAAATG GGGCCTGCCA 1080
AAACGTACTG TAAAAAAAAA AAAAATCTGG TGTCTTAGGC CCAGAGAGGG AAAAGAAAAT 1140
AAAGAAGAAA GAGTCATAAT TTCACAGTGC TCTTCAAACC CTCTCCCCAG CTTACCTGGA 1200
AAAGAAAAAG CCTTCAGACT CTTCACCACG ACAGAGCCTG CCAGGCTTGA AGAAAGCTAC 1260
AGCCTTGGGA TGGTCCAGTT CTCAGAGTCT TCATAGTTAC TTGGTGCCAA GAGCTTAAAA 1320
AGAGGAGGGG TGGTCGGGGA AAGTTGAAGG AGGACAGCAC GGGGGGAGAG AAAAAATGAA 1380
CAGAAAGGGA CCCAGGATAT TGAACAAGTC CTTTGACGAG CTTTAAATGG GTGAGGCATT 1440
GCTCATAGGG AACCCGCAGG AGCCCACACC AGTTCCATGA GTATTGCATG AGCCCAGCAG 1500
GGGCTAGTGA CTTCCAGCCA ATGGCCGAGC CTGCTTCGTA AGCTTTTCTG ATGGCCCCAG 1560
CAAAACCAGC ACTGTCTCAG GCCTCCACCA TGCCCTGTGG GTGTTTGGGC CACAGACTGG 1620
ACAACAAGGA CTTGTGCAGA AGGACATCGG ACTCTGGAGA GGTCTGAAAC AAGGGGTGGG 1680
GAGAGACAGG CTGGTCAGAG CTGCCTGCAA CCTCCCGTAT TCTCCTGGAT TGGCCTTCCA 1740
AAACCCGGGC TGACAGGCTC TTGGTAGGAA AACAGGCCCA GCAAACAAAG GTGTTCTCAA 1800
GCCCAGTTCA GTCACTGCCT CTGTCCCATG CTCTTAGTCT CATGGCTCTC AGGAGCAGGA 1860
CACAAGAGAC GGTTATGCCC AAGCACAGAA CACTCTTGGA AAGCCATCCT TTCCCTTCTG 1920
CTGACATTCT GACCCCCTCA AGGGTTGTCC ATGGGGAACA GGCTTTCTGC ACCCAATTGA 1980
CCAAAAAATA ACAGAAGCCT TCTCCTTAAG AAAGAGAGCA GGCCAGACAC AGTGGCTCAC 2040
GCCTATAATC CCAGTGCTTT GGGAGGCTGA 2070
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