EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS197-02161 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr1:235090470-235093080 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs908327chr1235092600hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr1:235091354-235091369AGGGGGCAGAGGGCA+6.63
Nr2f6(var.2)MA0728.1chr1:235092071-235092086GAGGTCATGAGTTCA+6.26
RARAMA0729.1chr1:235092071-235092089GAGGTCATGAGTTCAAGA+6.12
Six3MA0631.1chr1:235091720-235091737GCAAATGATACCCTTTC-6.12
ZNF263MA0528.1chr1:235091129-235091150GGAGCAGCTGGAGGAGGGGAG+6.02
Number of super-enhancer constituents: 69             
IDCoordinateTissue/cell
SE_00182chr1:235089787-235092321Adipose_Nuclei
SE_00983chr1:235090315-235091537Adrenal_Gland
SE_00983chr1:235092569-235093035Adrenal_Gland
SE_01666chr1:235090775-235091665Aorta
SE_01666chr1:235092553-235095108Aorta
SE_02305chr1:235090797-235091817Astrocytes
SE_04136chr1:235091089-235091897Brain_Anterior_Caudate
SE_06052chr1:235092563-235095925Brain_Hippocampus_Middle
SE_07547chr1:235089887-235092129Brain_Hippocampus_Middle_150
SE_09160chr1:235089274-235102029CD14
SE_13412chr1:235090132-235091861CD34_Primary_RO01536
SE_13412chr1:235092302-235095085CD34_Primary_RO01536
SE_14852chr1:235090111-235096258CD4_Memory_Primary_7pool
SE_19577chr1:235090565-235091808CD4p_CD25-_Il17p_PMAstim_Th17
SE_21117chr1:235090472-235092194CD8_Memory_7pool
SE_21117chr1:235092380-235094348CD8_Memory_7pool
SE_23314chr1:235090322-235090800Colon_Crypt_1
SE_23314chr1:235090805-235091803Colon_Crypt_1
SE_23314chr1:235092463-235096122Colon_Crypt_1
SE_23955chr1:235090350-235090759Colon_Crypt_2
SE_23955chr1:235090824-235091497Colon_Crypt_2
SE_23955chr1:235092554-235093067Colon_Crypt_2
SE_25800chr1:235089687-235101859Duodenum_Smooth_Muscle
SE_26806chr1:235090349-235091700Esophagus
SE_26806chr1:235092605-235093136Esophagus
SE_27663chr1:235089063-235101555Fetal_Intestine
SE_28576chr1:235088850-235101396Fetal_Intestine_Large
SE_29689chr1:235090283-235092133Fetal_Muscle
SE_29689chr1:235092238-235094048Fetal_Muscle
SE_31235chr1:235090341-235091774Fetal_Thymus
SE_31235chr1:235092263-235094078Fetal_Thymus
SE_31572chr1:235090061-235091822Gastric
SE_31572chr1:235091850-235096149Gastric
SE_32492chr1:235088942-235092206GM12878
SE_33758chr1:235092170-235101690HCC1954
SE_34767chr1:235092103-235099043HeLa
SE_36952chr1:235089804-235094553HSMMtube
SE_40307chr1:235092364-235094852K562
SE_40653chr1:235089852-235091891Left_Ventricle
SE_41640chr1:235092557-235093028LNCaP
SE_42265chr1:235089721-235091735Lung
SE_43462chr1:235092226-235096141MCF-7
SE_44805chr1:235090559-235091810NHLF
SE_45558chr1:235090190-235094180Osteoblasts
SE_47119chr1:235087515-235103374Panc1
SE_47599chr1:235090912-235091521Pancreas
SE_47599chr1:235092519-235093108Pancreas
SE_48697chr1:235089896-235091719Right_Atrium
SE_50040chr1:235092229-235094403RPMI-8402
SE_50071chr1:235089709-235100691Sigmoid_Colon
SE_51271chr1:235089831-235092066Skeletal_Muscle
SE_51271chr1:235092438-235095754Skeletal_Muscle
SE_51773chr1:235090507-235091828Skeletal_Muscle_Myoblast
SE_51773chr1:235092334-235094038Skeletal_Muscle_Myoblast
SE_52352chr1:235089712-235101497Small_Intestine
SE_53330chr1:235089854-235092349Spleen
SE_54553chr1:235090275-235096009Stomach_Smooth_Muscle
SE_56068chr1:235090847-235091959u87
SE_56760chr1:235090862-235091499VACO_400
SE_56760chr1:235092552-235093115VACO_400
SE_59259chr1:235089283-235124733Ly3
SE_60969chr1:235059965-235155853HBL1
SE_61435chr1:234961094-235124239Toledo
SE_62329chr1:235047040-235185428Tonsil
SE_63542chr1:235090473-235091948HSMM
SE_63542chr1:235092307-235094054HSMM
SE_65393chr1:235090044-235091867Pancreatic_islets
SE_65393chr1:235092372-235101616Pancreatic_islets
SE_67736chr1:235090847-235091959u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1235090546235090894
chr1235091073235091332
chr1235091427235091813
Number: 1             
IDChromosomeStartEnd
GH01I234953chr1235089124235101946
Enhancer Sequence
GCCCCAGGGC ATGGCTGTCT CCAGCCGCTC TGAGTAGCCA GCGGTGCAGC CAGCTGGTCT 60
CAGATTTGGG CTGTGATGAG TCTGGATGGC AGAAGAACAA GAGGGATGGG AAATTGAGGG 120
AGGGCCTCAT TGAAAGGGCT CACTCCAGGA GCCAGAAAAC CAGAAGAGCC TAAGGGACCC 180
AGAGCTAGAG TGAGACCAGA GATGCACAGT CCCCATGAGG ACAAAGAGCC CAGTGAGGAG 240
AAAGGGAGAG GTAAAAGGAT AAAAGAGTCA GAAGGAGTTT CAGAATCTAA GAGCTCCAAA 300
AATAAACCTT TCCCTTTGTA TCACTTTTCT CTTTTTACTT TAGTTGCTCT CAACTTGCTG 360
CTTCCTTTTT TTAAAAATTC TAGCAATTCT GCAGGAAACC AGAAGTGTGA ACCAAACACA 420
GTAACTCTAG GTGTTATGGC GCTGTCCTGC TCACCCTTCT TTTGGCCTAC TGGCTTCAAA 480
GGTAGGCACA CACACCGTCC CTTTTCTAAT GATCCGGTCG TGGATTCAGG CTCAGTAAGC 540
CAAGACCACA AGCAACAGGG CTTGGGCTCC ATCTGCCTCG GCTGCTTGCA GCTGCCTTCC 600
AGGAAGTGCT GGAACAGCAG AAGCAGCTAG CAGTGCGCTC AAGAAGTGGT CAGCAGTTGG 660
GAGCAGCTGG AGGAGGGGAG GCCAGTGAGC AAGTATCAGC TTGGGAAATA GGGTTTCGGC 720
TGAACAAAGT TCACTGCTGT TTTCTGAGAA AGCAGAACCT AGTGGAGCCA CCCTAGAGAA 780
TAAGGAGAGG AGCAACTGGA ACTGAGTGTT GGCTCCAAAC TTCCACGGCA TGATATGCTT 840
GGCCACCCAA TTGTGATCAG GGCCATTGTT GTTCCCCTGG GGGCAGGGGG CAGAGGGCAG 900
GCCGCCGCTC GGAGTAAAAA GGGAAGACAG ACAGGCAGTC CAAACACCAC CAAATGACAG 960
AGATGCAGAC CAAGACAAAA GGAAAAAACA ACAGAAGGGA TTTTTGTCCT TGAGACGTGC 1020
TATGCAAATT CTTTTCAATT AGTTTCCTAT TAATGATTCC ATCTTGAACA TTTAGAGCTG 1080
CTCAACCCAG GCAGCATCTA CGTTTTGAAG TAGTAAGTTC TCCATTCCTA GCAGAGTCGG 1140
AGGAGAAGCT CAGCTGTTAT CCACCAGAAA TTCTATTAAA AGGATGAAAG GTTGAACTAG 1200
ATGACTTCTC ATTCTGAAGA CTGTAATTCA GCAGAACTGA CTAATCCCTG GCAAATGATA 1260
CCCTTTCTGA GTATGCATGT GTCACTGAAA GTCACTCAGA CAAACCAGAC TATTTGTAAA 1320
TAGGTCTGAT TATCTGCAAA TTAGTTGATT GAAGGTTCCC GGGTATCAAG CAGGGCTTAT 1380
TTTAAGAAAT TAAGTTAATT TAGATAATAG CTGTGTTGAA AAGCAACAAG TTCAAAAACA 1440
ATTAAAAAGA ATGCAGCTTC CCTTTTATTT TTTTCAACTC TATATTTTCT TTTCAAATTG 1500
CTTCTAATAG ACCATCTGTT AAGAAAGCCT CTTTTGACCG GGTGCAATGG CTCACACCTG 1560
TAATCCCAGC ACTTTGGGAG GCCGAGGCAG GTGGATCACC TGAGGTCATG AGTTCAAGAT 1620
AGCCTGAGCA ACATGGTGAA ACCCCGTTTC TACTAAAAAC ACAGAAATTA GCTGGGCGTC 1680
GTGGCACGCG CCTATAAACC CAGCTACTCT GGAGGCTGAG GCACAAGAAT TGCTTGAACC 1740
CGGGAGGCAG AGGTTGCAGT GAGCTGAGAT AGCACCATTA CACTCCAGCC TGAGAGACAG 1800
AGCAAGACTC CATCTCAAAA ATAAAAAAAA GAAAGGCTCT TTCGTAAATT ACTTAAATAT 1860
GCTTAGAAGT CATTATTACT TTTTAAGTCA ATAGAAGTCT TTTTAGTTTA TCTAATAGCA 1920
TATTAATTCC TATGCTTTAT GTGTTTGTAC CCACACAACA CCCAGCCCTG CACCTAACAC 1980
ATAACAGGTG CTCAATAGAT GTTCATTGAA TAAATTGGTT GCAAAAACCG AGTGTATACA 2040
TTGAACATTT CTGCATATTG GTGATAATAA TAGTATTTTG AACACTTGTT CTATGCCAGT 2100
GACTGGGTCA AATAAACACT CAACCTCATA GTAATATCTG CGAAGTGATT GCTACATTAG 2160
CCCCATTTTA CAGATGATGC AACTGAGGCT GGTGAGAGGC AGAGCCAGGA TTCAAGGCCA 2220
GGCCTGTCCA ACTCCCGAGC CGAAGCTCTC AGCGAGGGTA TCAAACTGAA TCTGAATCCT 2280
CTTAGTTTAT CTATTTTAAA GTGCTGCATG TGGTATGTTC AGGAGACGAA AACTCTCTGA 2340
TGAGGCACGT GTGGATGGGA TGGCAGGGCT GAGAAGGCCG GCTCCCCCAC GGGGTGTGCA 2400
CAACCTACCT CCCCAGCTGT TTCTGCTACC GGCTGGGGCC TTCAACTCCA CCGCCTCCCC 2460
TCCCCCAGGC CCTAAATCAC TCTCAGGCCT TTTGTTCTTC CCCACAGCTG CTCAGCAAAT 2520
TCCTTGATTT GAAATTACGA TCACAGGTTG GAGTGCTACT TAAAATAATT TTGCCAAATG 2580
TTCCATCTCT CTGTGTTGAT GAATATAATG 2610