EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS061-08066 
Organism
Homo sapiens 
Tissue/cell
GM12892 
Coordinate
chr15:67384750-67386840 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr15:67385572-67385583TTCTTATCTGT+6.14
Gata1MA0035.3chr15:67385572-67385583TTCTTATCTGT+6.62
KLF16MA0741.1chr15:67384822-67384833GCCCCGCCCCC+6.02
KLF5MA0599.1chr15:67384822-67384832GCCCCGCCCC+6.02
SP1MA0079.4chr15:67384819-67384834CAGGCCCCGCCCCCA+6.56
SP4MA0685.1chr15:67384819-67384836CAGGCCCCGCCCCCAGG+6.14
ZfxMA0146.2chr15:67384819-67384833CAGGCCCCGCCCCC-6.19
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_02918chr15:67386179-67386773Bladder
SE_09181chr15:67382144-67387954CD14
SE_10181chr15:67382281-67388062CD19_Primary
SE_10875chr15:67354078-67404812CD20
SE_11885chr15:67382701-67385149CD3
SE_13896chr15:67382641-67386881CD34_Primary_RO01536
SE_14469chr15:67382077-67388724CD4_Memory_Primary_7pool
SE_16989chr15:67382866-67385219CD4p_CD225int_CD127p_Tmem
SE_17822chr15:67381944-67386311CD4p_CD25-_CD45ROp_Memory
SE_18371chr15:67382662-67386123CD4p_CD25-_Il17-_PMAstim_Th
SE_19163chr15:67382718-67385487CD4p_CD25-_Il17p_PMAstim_Th17
SE_20091chr15:67382587-67386972CD56
SE_21129chr15:67382353-67385662CD8_Memory_7pool
SE_22489chr15:67382945-67385445CD8_primiary
SE_26536chr15:67385707-67386928Esophagus
SE_31411chr15:67384110-67385093Gastric
SE_31411chr15:67385559-67386954Gastric
SE_32497chr15:67382687-67386215GM12878
SE_35858chr15:67382924-67385071HMEC
SE_36917chr15:67381009-67385968HSMMtube
SE_37941chr15:67379448-67386444HUVEC
SE_40033chr15:67381273-67385909K562
SE_44749chr15:67381210-67385562NHLF
SE_44749chr15:67385637-67386849NHLF
SE_45534chr15:67371483-67404480Osteoblasts
SE_47100chr15:67357928-67475420Panc1
SE_48052chr15:67380116-67385883Psoas_Muscle
SE_50064chr15:67381249-67386838Sigmoid_Colon
SE_52344chr15:67382553-67385154Small_Intestine
SE_53518chr15:67385112-67386847Spleen
SE_58377chr15:67342858-67447290Ly1
SE_59897chr15:67354926-67408793Ly4
SE_60508chr15:67357006-67428179DHL6
SE_61631chr15:67357404-67427415Toledo
SE_62286chr15:67356723-67443338Tonsil
SE_64236chr15:67385610-67387740NHEK
SE_65752chr15:67383689-67386908Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr156738512367385677
chr156738567867386334
chr156738582767386130
Number: 1             
IDChromosomeStartEnd
GH15I067079chr156737157467387927
Enhancer Sequence
GTTCTCAAAG TGTGGCCCTG GGCCAGCAGC GTCAGCATCA CCAGGGAACT TACTAGGAAT 60
GCAGAGTCTC AGGCCCCGCC CCCAGGCCTC TTGGATCAGA AACCCTGAGG GCGGTCCCAG 120
CAGTCTGAAT TTTGTACACT CTCCGAGGGC TGCTGATGTG CATTTGAGCT TGACAATCAT 180
GATTATAGGC AATGATGCAC CGTGTGGAAG CTGGGGGCAG GATACTGAGG AGGGTGCTGG 240
GGGTAGGAGT GGTGGAGGGA GTTTGTCCAG GGGAATGTGG TGTAGCGGAA AAGGCACAGG 300
ACTGGTAGGG CTGTGCCCCT TTAGGCCCAA GCCTGCCCTT GCTCTTAACC TCTTAATGGG 360
TTTCTTCTTT CTTCTGTTAA ACAGCTAAAA ATATCAAATC ATGGGGTTGC TGTGACGGTT 420
AAATGTAATA ACAGGCACGA TGTTCCATAT ATGTTGGGTC TTCTGGAGCT TTGGGGAAGG 480
AGGTGTGGCA ATAACAGCCA GCTTCTGCAT CATGGAAAAT GGCCCCCATG CCCATCCCTG 540
AGTTGTGTGG TCTGAAAATC AATGATGAAC ACTTAGGAGG CTTGTAGCCT GCTTTGAGTC 600
AACAGGAAGA CTGGACTTGA GAGTTTGGAA TCTATAGTCT AACTTCCCTT CCTCACCCTG 660
TCTTTGTAAA TGGTGCTCAT CTAACCCTAC AGTTACTATC TTTTCACTCA TGTCTAGCCA 720
CTTGTTAGAG GGGAAGGAAC CCTGGTGTCA GGACAGGACT CCTGGCTCCC TGAGCTTGCT 780
GTGTATTCCG GGGCATATCC TTAACCTCTC TGAGATGTAC TTTTCTTATC TGTAAAACCT 840
CTATGTTGAT GCAAATCAGG TGCGATGATG GACGCAAAAA CTGCCTTGAA CACCTTAGCG 900
GGCCTGTGAA TATAAAGCCT TCAGGATCCA CACCTCTGCC AGGGCCCACA CCAGCCTCGC 960
CACCTCGGTG AGCCTCTCAT TCCACTGCCA GTGCAGGGGT GCATAATCAG GATTTGCCAG 1020
TGGAGGTAGG AAGGGTGGCT GGATTGTGAC TGTCACGCTC CTGGCATCAG ATGATACTGG 1080
TAGCAAGCTA GGGTCGTCTG TGCACTTTGC TCTCTCTCAG TCTTCCCAGC AGCCCTGTCA 1140
AGCGGGGAGT CTAGCAAGAA GTGGCCAAGG CGCAGATCAT TTAAGAGGAA GGATGTGAGC 1200
AAACTGGATC CCAAGGGGAC AGACAGAGGC CCACTTTGCC TCAGAGTCCA GAGAGCTGCT 1260
GCTGCTAAGA AGGGAAAGAG GAACTGGGTC GGGGTGCCTG CTGACTTGCA GCGCTGTGTT 1320
GGCATGCGAG GTAGCACTGG TTGGGAGGCG GTTACCTGAA GGAAGCAAAG GCAGCTGGTG 1380
GTTCCTATCT TCTTGCCTCT GGCAGCACCT AAAAGAAGCC TCTTGGGCCA ATGAGAGGAT 1440
GGACTGTCCC CCACCTGCAG AGTTCTGTGA AGTGGTGCGG ACGTCTTTGT TGATCTCATT 1500
TGGTGCCTCC CCCTGTTGAT GGCTGAGGAA GCCAAGGCTC TGAGAAGGCA CATGGTTTAC 1560
CCGAGGGGAC ACAGGCAAGG AATCTGAACC CGGATTGCAT TTTCTGTTTT AGGGCTCTTT 1620
GTGTGACCAC GGTGCTTCCC AGGCCCACAC TTCCAGTGTT CCAGGCCCTT GACCACCAAT 1680
CCTGTGGAGG GGTCCTCAGG GCAGGCAGTG GGACCACCTG AGGCCTGCGT GGGGTGGCCT 1740
GTGGTGTGAG GGACCCAGGA AGTCAGCCTG CACCTCGGCG AGTCAGAAGA TGTGGCCATC 1800
CACCAACCAT CAGATGTTCC CCTACGCTTA GGGCTGTGAC CAGAAGTGGC ATCAAGATGG 1860
GAGGCGAAGC TTCTGGGACC AGAGAACCAG CTGCTCCTGT TCATCCTGCT TTTGGGTGAA 1920
TAGCTGATGC TCTGGGCCCC TCATCCCACC ATCCCACCCC GTGGCTCCTC CTGAGCAGGG 1980
CTGAGGGCAT TTACCTGGCT GCCTTCTAAA GCAGACTTGG CACGAGACAA TCTTATTCAA 2040
ACTCTGCTCA AAATTGCTAC CCTGAGGAGA GGGCTGTGAC CAGGCAGGAC 2090