EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-09480 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr17:43369870-43372390 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs721579chr1743370481hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr17:43371336-43371351TGGACTTTGGTCTCT-7.31
LMX1BMA0703.2chr17:43372217-43372228TTAATTAAAAT-6.62
MYCMA0147.3chr17:43370615-43370627GGGCACGTGGCT-6.18
PAX5MA0014.3chr17:43370191-43370203GAGCGTGACCTC+6.14
RREB1MA0073.1chr17:43371155-43371175TCCCCAAACACCACCTCCCA+6.67
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_01249chr17:43369797-43372371Adrenal_Gland
SE_04602chr17:43367359-43372240Brain_Anterior_Caudate
SE_11470chr17:43364690-43370274CD20
SE_11470chr17:43370585-43396257CD20
SE_15206chr17:43369767-43372845CD4_Memory_Primary_7pool
SE_18500chr17:43366366-43375242CD4p_CD25-_Il17-_PMAstim_Th
SE_19630chr17:43370599-43371979CD4p_CD25-_Il17p_PMAstim_Th17
SE_23493chr17:43370233-43371784Colon_Crypt_1
SE_24167chr17:43370547-43371576Colon_Crypt_2
SE_25878chr17:43364447-43377187Duodenum_Smooth_Muscle
SE_26725chr17:43369959-43372440Esophagus
SE_30018chr17:43370009-43372329Fetal_Muscle
SE_31611chr17:43370038-43372444Gastric
SE_32589chr17:43370933-43372485GM12878
SE_34075chr17:43370326-43375105HCC1954
SE_40748chr17:43363700-43375200Left_Ventricle
SE_41691chr17:43369983-43371993LNCaP
SE_44657chr17:43370169-43372693NHDF-Ad
SE_46201chr17:43369956-43372823Osteoblasts
SE_47195chr17:43366097-43378703Panc1
SE_48714chr17:43365874-43374860Right_Atrium
SE_49545chr17:43369873-43372224Right_Ventricle
SE_50169chr17:43369845-43372240Sigmoid_Colon
SE_51970chr17:43369906-43372027Skeletal_Muscle_Myoblast
SE_54723chr17:43359357-43378642Stomach_Smooth_Muscle
SE_59053chr17:43370566-43412054Ly3
SE_62481chr17:43366079-43396493Tonsil
SE_63770chr17:43369873-43372185HSMM
SE_65719chr17:43369005-43372029Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr174337097443371161
chr174337014743370559
Number: 1             
IDChromosomeStartEnd
GH17I045290chr174336802843375075
Enhancer Sequence
GAGCTGAGAT TGCACCATTG CATTCTCCAG CCTGAGTGAC AGAATAAGAC CCTGTCTCTA 60
AAAGAAAAAA AAAGTCTAAG GGGTGTTCTG ACATCCAATT AGGCAAAAGC CCTTCAAGGC 120
TGGCTATGCT TCTTGTAACT GTACTTTCAT CCCACCTCAC ACCTCCCCAC CCCACTCTAC 180
CTCCAAAAAA GAAACTGACC TAAGCCCAGA GCCGATCCCA CTGTTCTCAG CCTCTTTACC 240
AGGGGAAATG AGATCTTAAG AACAGACCAA AAAGTCTCCA AACCTAACAG CAGTAGGGAA 300
TGCTCACAGG GAGCTCGATG TGAGCGTGAC CTCCTCATTT CTATTTGAAG AAGCTGAGGC 360
CTAATTCAGT GGAGACTTGC CCAAGGTCAC CCAACCCACG TGTGACAGGA CATGGCCAGG 420
ATCCAGACCC TAGGTTCTTT AGGCTATGAT GCCCACTCCC CAAGCTCCTG GGTTACAGGC 480
AAATGCAGGA GGGCACACTA AGGTCCTCCC TGGTCAACAG GCTCCTGAGG GAAGAGGTGG 540
GGCCCTGCAC ACAGTGCCTC CCCAGTGTAT AGCACAGGGG CCACAGACCA CGCAACTGAC 600
GCTGGCTGAA CGAGGGACTC AAAGGACAAA GATTGCTTTT CCATAACCTT TGGAGACAGG 660
ATGATCCCGA ATGCTGAGGA GGAAGAGAGA GTCCTGCCTG ATGAATGAGA AAAATGAGGC 720
CAGGTGGTGC AGTTGCTGCT CTGAGGGGCA CGTGGCTATT AGAGATCTGG CTGTGTGGGG 780
GCTCTGATAG CCTGTCTCCG CCTGGCATGG CCCAACGGAG GCTTCTGGAT AGGTCATCCT 840
GAGCTAGAAC TCCTCCAGAG GGGGTGCAGG GCATCCCGAG TCCCAGAGTT GTCCTTTCAT 900
ATTGGTGTTA GGTAGGCAGC TGTCCAGCGC CCCTCTGTGA GCACACCAGG CTCCCCTCTT 960
CCCAGAGAAG TGGAAGCTGA GGCTGAGGCA GCCACGCTCA GAGACTCCTT TGCAGTTCCC 1020
CGATGACTCA TCCAACAGCC TGGCAGGCAG ACAGTAACAA GGAGGCTGTT GAGAAGCTGA 1080
CCCAGCAGAT GGCAGCTGAA CTTGTGAAGG ACATGGGGAA AACAGGCTGA CCCTCACCTC 1140
TCAGGGGCAC AAATCACGGC CTGGGAGCTG TAAAGCTCCT CCTGTGGCTG GCTTTTCTGT 1200
GCCACATCAC CATGACTCAG ACCCTCACCG ACAGCCTCCA AGTTCAAGAG GCTATTCTTG 1260
GGACACTTTG GCCTGACAGT GGCTCTCCCC AAACACCACC TCCCACACAG ACACACATGC 1320
ACACACACAC ATGCACACAC AGACACACAC ACATACGGAT GCACTTGCTC CCTCCCTCCT 1380
TTCCTAATTC TATCTGGACT CTGGTCTACA AAAATCATGG TTCTGTACTA AGTCCAGGAC 1440
TACTGGCCAG GGGGCCTTCC CAGCCCTGGA CTTTGGTCTC TGGCTGTCAC CCCAGCTCAT 1500
GGCCCTAACA CTTTGCCCCT TCTCCCTCCT GCAGCGTGTG GGGAGGACGA AGTGGGAGCC 1560
AGTTATGTCT CTGCCTTTGA AGGCAAGTCA AACTCCTGAT TCATTCCTCA GCCTAGACAC 1620
TCTCCTCAGC TTATTCACGC CCCAAAGGCA TTGGGCCCTC TACTCTCTGC ATAAGAGTTG 1680
AGGACACGAG CAGTGGCAAC AGCCAAACCC ACATGGCTCA CCCATAAGCC CAAGAAATCA 1740
GAAGAGGAAA GGAAAGGAGC AGAATTCACT CCATATTCTT TGAGGCCTGA TGCACAGACA 1800
CTGTTGGTTC TTTCTTCTGT GATGCCTCAG TGACCTCCTG GAGAAGCCTG GGGGATAGGA 1860
ATGATCTGGA CAGTACCAGA TCAACCTCTG GGCATAGCTG TATGAGGAGT TCTTAATCTA 1920
GGTTCAAGGA TGGATTCAGG GAGAAAAATG TAATTTGCAT TTTTCCAGGG AAGACTTGGT 1980
CCATAGCTTT CAACAGATTC TCCAAGGATC TGCCATTCCC CAGAAGGTTC CTCTAGTCTC 2040
CCTAGAAAAT CAGGGCCGGG CTAAATGCCT GATTCTGGCT CTATTCTTCC ACTCCGAGGA 2100
AAAGCTCTCC AATGCAGCAG TTTCCAATCT GACCACAGAT TAGAATAACC AGATAAGTTC 2160
TTTAAATGCA TTCCTCCTAG GCCTGCTGAA CCAGTCACTG GGCATTAGGC CCAGAATCTG 2220
TACTTTTGAC AAGTTCTCTG GATGATTCTG ATGCCAAAGG GCCAGAGACT GCCACCTGAC 2280
CCCTGCTCTG TACTCAAGGC GACACTGTCC AAAATGGTAG CCACTAGCAA CATGTGGCTA 2340
TTTACATTTA ATTAAAATGA GGTAAAATTT TAAAATCATT TCCTTGTTAC ACTAGCTACC 2400
ATACTCAACA GTGCAGACAG AGAACATGTC CAGCATTGCA GAAAGTTCTA TTGGACAGTG 2460
CTGTTCTGAG GTGATGAGAG CGGTGTTTTC TCTGACAGTA AAATTTCTGT TCCTAGGATT 2520