EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS093-15097 
Organism
Homo sapiens 
Tissue/cell
HL-60 
Coordinate
chr19:11202930-11204850 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr19:11203473-11203485GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr19:11204803-11204815GTTTGTTTGTTT+6.32
SPI1MA0080.4chr19:11204085-11204099TACTTCCTTTTTTT-6.3
SPICMA0687.1chr19:11204085-11204099TACTTCCTTTTTTT-6.79
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_01022chr19:11202909-11203678Adrenal_Gland
SE_01022chr19:11203682-11206319Adrenal_Gland
SE_12085chr19:11199436-11204174CD3
SE_14622chr19:11198676-11207877CD4_Memory_Primary_7pool
SE_17142chr19:11199458-11204099CD4p_CD225int_CD127p_Tmem
SE_19715chr19:11199366-11204828CD4p_CD25-_Il17p_PMAstim_Th17
SE_20994chr19:11198676-11207604CD8_Memory_7pool
SE_22774chr19:11199079-11204103CD8_primiary
SE_23239chr19:11198937-11203807Colon_Crypt_1
SE_23239chr19:11203891-11206070Colon_Crypt_1
SE_24095chr19:11201137-11203799Colon_Crypt_2
SE_24095chr19:11203945-11204272Colon_Crypt_2
SE_24095chr19:11204321-11204812Colon_Crypt_2
SE_24928chr19:11199034-11204236Colon_Crypt_3
SE_24928chr19:11204281-11204823Colon_Crypt_3
SE_26902chr19:11198490-11204883Esophagus
SE_28429chr19:11198835-11207741Fetal_Intestine
SE_29308chr19:11199027-11207595Fetal_Intestine_Large
SE_29905chr19:11198697-11204091Fetal_Muscle
SE_31737chr19:11199668-11204904Gastric
SE_34726chr19:11198191-11208606HeLa
SE_36050chr19:11198460-11204893HMEC
SE_38264chr19:11198668-11208150HUVEC
SE_40068chr19:11198411-11207591K562
SE_42817chr19:11199051-11207805Lung
SE_44493chr19:11198423-11203875NHDF-Ad
SE_44932chr19:11198436-11204000NHLF
SE_44932chr19:11204002-11204881NHLF
SE_47094chr19:11203332-11203713Ovary
SE_47094chr19:11204371-11204735Ovary
SE_47693chr19:11201130-11203607Pancreas
SE_47693chr19:11203842-11204276Pancreas
SE_47693chr19:11204321-11204840Pancreas
SE_49361chr19:11199614-11203237Right_Atrium
SE_49361chr19:11203270-11203861Right_Atrium
SE_49361chr19:11203878-11204812Right_Atrium
SE_50772chr19:11198863-11207767Sigmoid_Colon
SE_52540chr19:11198883-11208401Small_Intestine
SE_54059chr19:11198844-11207806Spleen
SE_57847chr19:11202662-11203691VACO_503
SE_64571chr19:11198697-11204072NHEK
SE_64571chr19:11204114-11204825NHEK
SE_65732chr19:11198652-11207882Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191120296311203178
Enhancer Sequence
CCTTTTCCTT CCACACTCTG TCCCAACTGT CAAGCAAATA GCCTTTTGTT GCTAAGAGAC 60
TGCAGATGTA ACCGACCAGC AGCAAACAGT GAGTCAGGCT CTCTCTTCCG GAAGCAAAAT 120
CAATTGCTGA GATCACTCTG GGGAAAATAC CCACCTTATT TGGAAAGAAG CACTGATCAA 180
TTGATGTCTA TTTTTTTTTT TTTTGAGTTG GAGTCTCGCC CTGTCACCCA GGCTGGAGTG 240
CAATGGCATA ATCTCGCCTC ACTGCAATCC CCGCCTCCCG GGTTCCAGCA ATTCTCCTGC 300
CTCAGCCTCC TGAGTAGCTG GAATTATAGG CGCCTGCCAC AACACCCGGC TAATTTTTGT 360
ATTTGTAGTA GAGATGGGGT TTCACCACGT TGGCCAGGCT GGTCTCGAAC TCCTGACCTC 420
GTGATCCACC CGCCTCAGCC TCCCAAAGTC CAAGGATTGC AGGCGTGACC CACTGTGCCA 480
GCCAATCAAT TGATTTCTCA TTCATTTTCA GCTGGCTCTG TTCCCTTAAG CCAGGGGATT 540
TTCGTTTGTT TGTTTCCCCT TCAAGGAAAT GATTCTAGCT ACAGTTTTGA TTTCCTTGTA 600
CAACTGTTTT CAGTAGCACA GGGAAAGAAA ACATCGAAAG CATTCACCAC CTCATTTGTG 660
TGCTGGGGGA AAAAGCAGAA ATGTGTATTC TCTTTTTTTG TTTCGATGAC CTTGTTCCTG 720
ACTTGTTACT CGTGACTTGA GAGATCAGAG GGCTAGAGGA CTAGAATTTA TAGAGGTGTT 780
TTTTTTGTTT GTTTATTTTT GTTCGAGTTG CCCAGGCTGG AGTGCAGTGG CGCAATCTCG 840
GCTCACTGCA ACCTCTGCCT CCCAGGTTCA AGCGATTCTT CGGCCTCAGC CTCCTGAGTA 900
GCTGGAACTA CAGGCGCCCG CCACCACACC CAGCTAATTT TTGTATTTTT CAGTAGAGAT 960
GGGATTTCAC CATATTGGTC AAGCTGGCCT CGAACTCCTG ACCTCGTGAT CCACCCGCCT 1020
CAGTTTCCCA AAGTGCTGGG AGTACAGGCG TGAGCCGCCG TGCCCGGCCT TTTTGTGTTT 1080
TTGTGTTTTT GAGAGGAGCT CATTGCTTTT TAGGCTTCCC TAGCGTGAGA AAATCTGGGG 1140
ATCCATGCTC TAGTTTACTT CCTTTTTTTT TTTTTTTTTG AGATGGAGTC TCGCTTAGAT 1200
TGCCTAATCT CAGCTCATTG CAACTTCTGC CTCCGGGGTT CAAGGGATTC TCGTGTCTCA 1260
GCCTCCTGGG TAGCTAGGAT ACGGGCACCC GCTACCATGC CTGGCTAATT TTGTACTTTT 1320
AGTAGAGACA GGGTTTCGCC ACGTTGGCCA GGCTGGTCTC GAACTCCTGA CCTCAGGTGA 1380
GCCGCCTGCC TTGGCCTCCC AAAGTGCTGA GATTACAGGC GTGAGCCACC GCGCTTGGCC 1440
TAATTTGCTT TTCCTGAAAT TCAAATGGTC TAATATGAAA AACGCCAACC TTGCTTGAAA 1500
GAATAAGAAA GAGGTGCGGT TTCGTTGGGC CGTTGATGTT TGGAACAGGA CTGGTTTTGT 1560
CCCCTTGCTC GGAAAGGGCA GCAACTGTGA GGACAGCTCC CTGACGTGCT CTCACTCAGC 1620
ACTGTTCCGT TCCTGAGCAC TGTCCCCACT AGCTAGGCCA AGGGAGCTCA TTTGGCAGGC 1680
AACTGCTGTC TGGCTGCGCC TGTGGCAGTA AAATCTGCCT TTATTTTTTG GAGGCAGGGT 1740
CTTGCCCTGT CGCTCAGGCT GAAGTGTGCA GTTATAGCTC ACTGCAGCCT CCAGCTTCTG 1800
TACTCAACTG ATCCTCCTCT CTCAGCCTCC TGAGTAGCTG GGACTATACG CACGTGTTAC 1860
CACTCCCACC TCAGTTTGTT TGTTTATTTA TTTATTTATT TATTTATTGA GATGGAGTTT 1920