| Tag | Content |
|---|
EnhancerAtlas ID | HS047-28359 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr6:7165260-7167590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr6:7165894-7165908 | GGGTGGGCGTGTCC | - | 6.09 | | Klf12 | MA0742.1 | chr6:7166739-7166754 | GAGCTGGGCGTGGTC | - | 6.2 | | SP8 | MA0747.1 | chr6:7165895-7165907 | GGTGGGCGTGTC | - | 6.02 | | Tcf12 | MA0521.1 | chr6:7167491-7167502 | CAGCAGCTGTT | - | 6.32 |
|
| | Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
| SE_00099 | chr6:7150760-7175124 | Adipose_Nuclei | | SE_09175 | chr6:7163784-7174861 | CD14 | | SE_13205 | chr6:7166140-7166829 | CD34_Primary_RO01480 | | SE_13456 | chr6:7163868-7167966 | CD34_Primary_RO01536 | | SE_14595 | chr6:7163085-7171913 | CD4_Memory_Primary_7pool | | SE_20929 | chr6:7163779-7167986 | CD8_Memory_7pool | | SE_23267 | chr6:7164631-7167596 | Colon_Crypt_1 | | SE_24175 | chr6:7165169-7165675 | Colon_Crypt_2 | | SE_24175 | chr6:7165789-7167567 | Colon_Crypt_2 | | SE_26179 | chr6:7164111-7167813 | Duodenum_Smooth_Muscle | | SE_26569 | chr6:7163998-7167669 | Esophagus | | SE_28374 | chr6:7164538-7168368 | Fetal_Intestine | | SE_29027 | chr6:7164378-7172529 | Fetal_Intestine_Large | | SE_30159 | chr6:7164609-7168319 | Fetal_Muscle | | SE_31471 | chr6:7163963-7167667 | Gastric | | SE_35642 | chr6:7163876-7167718 | HepG2 | | SE_37264 | chr6:7164374-7175164 | HSMMtube | | SE_39870 | chr6:7163818-7168464 | K562 | | SE_41219 | chr6:7164701-7166534 | Left_Ventricle | | SE_42377 | chr6:7164447-7167625 | Lung | | SE_45215 | chr6:7164678-7167696 | NHLF | | SE_46025 | chr6:7164033-7174855 | Osteoblasts | | SE_48253 | chr6:7163936-7166576 | Psoas_Muscle | | SE_48253 | chr6:7166589-7171816 | Psoas_Muscle | | SE_50177 | chr6:7163854-7167657 | Sigmoid_Colon | | SE_51588 | chr6:7164219-7171342 | Skeletal_Muscle | | SE_51921 | chr6:7164853-7167579 | Skeletal_Muscle_Myoblast | | SE_52972 | chr6:7164599-7167658 | Small_Intestine | | SE_53741 | chr6:7164948-7167710 | Spleen | | SE_54903 | chr6:7164533-7166261 | Stomach_Smooth_Muscle | | SE_63714 | chr6:7164931-7168475 | HSMM | | SE_65660 | chr6:7165807-7166909 | Pancreatic_islets |
|
| | 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 |
| GH06I007163 | chr6 | 7163921 | 7175032 |
|
Enhancer Sequence | ATGTCTAAGT GAGCCCTGAA AGTAAGTTCT CTTCTCGGAA GCATTGGCCT CTCACACACA 60
GAGGCACAAG GAGTGCTATC CGTTGGACTT GAAGGCTGTT AGAGTTGGAG CTGCAATGGA 120
TGCCGGGTAG GTGTTGCTTG GGCATTGTTC CAAGAGGCTC TGGAGGCAAA TATTTTAAAC 180
AAGTCAAACA GCCCCTCTAG GCGAGCTGCA GGAAGTCCAG CCCTTGCCTT CGTGTGGTCA 240
GCAGGAGATA AAAGTGTGGA CTGTTGGAGG CTAGGCCCCT CCTAACACTG GATAACAAAC 300
TGTTAAGGGA AGATAAAAGG AAAGAGTAGG GATGTCCTTT TTAAACAACA TGAAGGTGCC 360
TTTGTCACAT GCATTCAAGT AAATTACGGG TGGTGAGCAA GACATGCCTC ATTTTTATGA 420
TCACAAGCGT GTTGAAGAAT TCTGAGAAGC AGGACTTGGT TTCAAAAGTA TGCCAAAACA 480
ATTTCATGTC ATGAAAATAC TGGTAGAGGT AGGCTTTTGA TTGAGAATGT TCCCATTACA 540
TACTGGGTTA CATTAAATAG GCATCAGCTT GGATTTACAA ATCTGTGTGC TACAGAGATT 600
TTCCCTGTTA AGGTGTGTCT GACCCATGGG GACTGGGTGG GCGTGTCCAG CTGCCCTTGG 660
ACTGGGCAGA TGAGCAGGCA GGGCGGCTGT GCTTCTCTGA AGTGTGCGCA TCTCCTCTTA 720
GTTGTGCTTC TGGTGTTGAC CCAATTATTG CCCGGGTATG AAAGAGTTTG AAGGAAGAGA 780
CTGTCCTGCT GGTGTCTATC TCCCCTTTTC AGTTTTCCTT CCTGTTCTTT GTAACATTTG 840
GGGGGAGTTT GGGGGCTTGC AAAGGGGTTA TCTGTTTCTC AGGGTGGGGC TTGTAAACAT 900
GAACCCACAC TTAAGAGCCT GGGCATGTTC AGTGCCCTGT GTGAGCTCAA TCCAAAGCAA 960
GTGAACAAGT GTGCTTCAGG GACATGATGC TTGTTTCAGG CCCCGCTGGG CCGTGGAGGG 1020
GCGGTGGCCC TTTGTGCAGT TAGACCCCCC AGGGAGTGCA GTTGTGAACT AATCACCGCC 1080
TGGAGAGCCT GTGTGCCTCA CACTTCCTCC AGGACTGCAC TAATCCCCAC TCCCACCCCC 1140
AACTGCCAGC CCCTGGCCTT GGCCCCCTCC TTCCAAGGTG CCTCTGCTGG TCCAGGAACA 1200
TGCCACCTCC TCTCCCAGCT GCACATGGGC TTTCCAAAAA GGCCCATCCT GCCTGCTAGT 1260
CATTTTTGGT TTGCTCAGTT TACTTTAAGA AAACCCATTT GCTTGCCAGT GTTTTTGGTT 1320
GGCTAGCTTG TGATAAACAC TTATCAACCA CTTATATCTC AGAGCATTTG TTTTCCTTCA 1380
TATGCACAGT AGTAAATACT TTTCTTAGAG GCGAATTTGG GGGTGAGGGG ATGGGAGGTT 1440
TTCTGTTGTA TGGCGGAGGG CAGCCCATGC AGCTCCTGGG AGCTGGGCGT GGTCACTTCA 1500
CCGCACACAG TCATTCCCAG CTGACGGTTT GTAACGTCTG ATTACGCACT GTGAAATTTT 1560
GACCACAGCT GACCACTTTT CCAATGGGCG AGGAAAGATG TGATCTCCTC CTTCCACTGC 1620
CTTCTCTAAG CTAAGCTGTT AGGGGAGAAG CATTTCAAAC GCTTGTATCT TCCACAAGTC 1680
ATTTTGGTTT TCTAAGGAGT GTCATCCTGA ATTCTGGGAA TTCGAAGCCC AGATTTAAGG 1740
TAAATCACCT GCCCTGGGAT TGCTTAGCTT GCAGCTCGTC CCTGGGGCAA AGTGGAGAAT 1800
CCCGTTGCTG CTGCACCCTT TCCCTGAGCA TGTCAGAAAG GCCAGCCCGG CGACCTCAGG 1860
GCCTGTGAAA GAGTTGCAGG ATATTGCCTA AAACTCTATG CAAACTGCTA CTGAACTTTA 1920
CCCTAGCTTC TTACCAGAAG CTGGAAATGT GACCGAAGAT ACTTAGATTC ACTTCAGAGA 1980
TGTGTCCCAG AACACTCCCA TTTCTACCAT ACATTGTCAT GGTGTCAGCC ATGCTGTATT 2040
CAGGTGCTGC AGTTAGTTGG GAGAGAAGCA GCTTGGTGAA TATAGGGAAG AAAGAGCTGC 2100
ATCCCTGTGG CAGCCAGTAG TGTGTACTTC CGTAATTAAC CAAACGTGAA GCTGACCAGG 2160
ATTGGTTTCA GCAGCAACTG AAGTCAGAGG GGTTTTTATT TCCTGGTCGC CAGATAGCAT 2220
GGCGACTGTG TCAGCAGCTG TTCTCATTGG CCAGGGGATT GCATTTGGGA AAAGCCAAAT 2280
TATATTTATT TTAAATTGTC CAACTTGTGG GCTGGGACAG GATTTTTTTT 2330
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