| Tag | Content |
|---|
EnhancerAtlas ID | HS116-16875 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr19:11201210-11202850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr19:11201218-11201228 | GGGGCGGGGC | - | 6.02 |
|
| | Number of super-enhancer constituents: 36 | ID | Coordinate | Tissue/cell |
| SE_01022 | chr19:11199673-11202882 | Adrenal_Gland | | SE_12085 | chr19:11199436-11204174 | CD3 | | SE_14622 | chr19:11198676-11207877 | CD4_Memory_Primary_7pool | | SE_17142 | chr19:11199458-11204099 | CD4p_CD225int_CD127p_Tmem | | SE_19715 | chr19:11199366-11204828 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20994 | chr19:11198676-11207604 | CD8_Memory_7pool | | SE_22774 | chr19:11199079-11204103 | CD8_primiary | | SE_23239 | chr19:11198937-11203807 | Colon_Crypt_1 | | SE_24095 | chr19:11201137-11203799 | Colon_Crypt_2 | | SE_24928 | chr19:11199034-11204236 | Colon_Crypt_3 | | SE_26902 | chr19:11198490-11204883 | Esophagus | | SE_28429 | chr19:11198835-11207741 | Fetal_Intestine | | SE_29308 | chr19:11199027-11207595 | Fetal_Intestine_Large | | SE_29905 | chr19:11198697-11204091 | Fetal_Muscle | | SE_31737 | chr19:11199668-11204904 | Gastric | | SE_34726 | chr19:11198191-11208606 | HeLa | | SE_36050 | chr19:11198460-11204893 | HMEC | | SE_38264 | chr19:11198668-11208150 | HUVEC | | SE_40068 | chr19:11198411-11207591 | K562 | | SE_42817 | chr19:11199051-11207805 | Lung | | SE_44493 | chr19:11198423-11203875 | NHDF-Ad | | SE_44932 | chr19:11198436-11204000 | NHLF | | SE_47094 | chr19:11201114-11202030 | Ovary | | SE_47094 | chr19:11202151-11202773 | Ovary | | SE_47693 | chr19:11201130-11203607 | Pancreas | | SE_49361 | chr19:11199614-11203237 | Right_Atrium | | SE_50772 | chr19:11198863-11207767 | Sigmoid_Colon | | SE_52540 | chr19:11198883-11208401 | Small_Intestine | | SE_54059 | chr19:11198844-11207806 | Spleen | | SE_57847 | chr19:11200082-11202661 | VACO_503 | | SE_57847 | chr19:11202662-11203691 | VACO_503 | | SE_58185 | chr19:11201144-11202136 | VACO_9m | | SE_58185 | chr19:11202138-11202700 | VACO_9m | | SE_64571 | chr19:11198697-11204072 | NHEK | | SE_65732 | chr19:11198652-11207882 | Pancreatic_islets | | SE_68998 | chr19:11198847-11202870 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTACGAGCGG GGCGGGGCTG GCGCGGAAGT CTGAGCCTCA CCTTGTCCGG GGCGAGGCGG 60
ATGCAGGGGA GGCCTGGCGT TCCTCCGCGG TTCCTGTCAC AAAGGCGACG ACAAGTCCCG 120
GGTCCCCGGA GCCGCCTCCG CGACATACAC GAGTCGCCCT CCGTTATCCT GGGCCCTCCT 180
GGCGAAGTCC CCGGTTTCCG CTGTGCTCTG TGGCGACACC TCCGTCCCCA CCTTGTCCTG 240
GGGGGCGCCC TCGCCCCACC AGCCCCGATC AAGTTCACAG AGGGGCCCCC GGCCACCCTC 300
AAGGCCTCGG TTCCTTACGA GGTTGAAACG TTGCCTCAGA ATCTCCCCGC CCCTCCTTGG 360
TCTGCAGCCG AGATCTTCAG CCACGGTGGG GCAGCTATCC CCCGGGACCG ACCCCCTGGG 420
GTGGCCTCGC TTCTTCAGAG GCTGTGAATG GCTTCGGTTC AGCTGTCCAA GCGGCGATTT 480
TTCCTCTGGG TGAAATGGAT TAGATTTTAG ATTTCCACAA GAGGCTGGTT AGTGCATGAT 540
CCTGAGTTAG AGCTTTTTAG GTGGCTTTAA ATTAGTTGCA GAGAGACAGC CTCGCCCTAG 600
ACAACAGCTA CATGGCCCTT TCCCTCCTGA GAACCAGCCT AGCCTAGAAA AGGATTGGGA 660
TTGCCTGATG AACACAAGGA TTGCAGGAAA CTTTTTTTTT AATTGGCAAG GGGGTTGGCT 720
TTGACTGGAT GGAGAGCTTT GAACTGCCTT GAAATTCACG CTGTAACTAA CACACCAGTT 780
TCCTCTGGGA GGCCAGAGAG GGAGGGAGGG TGTAATGAAA TACGGATGAT TGTTCTTTTA 840
TTTTTATTTA CTTATTTATT TTTTAACTTT TTGTAGAGAT GAGGTCTCGC TTGGTTGCTC 900
AGGCTGGTCT TGAACTCCTG GCCTCAAGCG ATCCTCCTAC CTCAGCCTCC CAAAGTGTTG 960
GGATTACAGG AGTGAGCCAC CGCGCCCCAC CGGGGATGAT GATGATTGCA AACATTCTGC 1020
CACTCAGTTT TACAAAAGAA AGAGAGGCAC TGGATTAATG TGTATCTCAC TCACCAATCA 1080
ACCTCTTCCT TAAGAGAAAA TGTTAAGGAA GTCTTAGGCA AGGCCTTGTT TGTTCATCAC 1140
TTTAGTTTCT CTCTCCCGGG ATGGCTGAGA ATGTGATGTT TCCTCTGTTG TCAAGGAGAC 1200
TACACCCCTG ATGTTTTCCT CCAGACTTCT GAGAGCTGGT GTGTGTTTCT AGCACTTTCT 1260
AGCTGCACCA CCTCACGCTG TAGCTGGCTT CAAGGCATAT CCAGGGGGGA GTTTCTTGTC 1320
CATTTCCTTT ACAAAGGGAA GTTGTTGGAA TCTGAACCGC AAGCCTTCAC TTAGACCAAA 1380
ATCAGGCAAC AGCGGTGAGC GCAGCTCCAA ACGTGTCAAT GACTCACCCA AATTTGAGTA 1440
AGGGAGTTGG CTGCTTTAAC GAGCCGCAGG GTGATTCCCT TGTCATTTCC GGAAATACCT 1500
ATCTTCCAGG GAACACTGGG AAAAAACAGG GAGACCTTTG TTGAGACAGA AAACCTGTAG 1560
GGGAATTCTG TTCCTCATTC CTGCTCTTAT CTGTAGACTT CCTCCCTGAT AAGATCCAAT 1620
TCTAGATGGG TCGGTTGCTC 1640
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