EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS087-02664 
Organism
Homo sapiens 
Tissue/cell
HEK293T 
Coordinate
chr1:235097330-235098190 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SRFMA0083.3chr1:235097643-235097659TGCCCATATATAGGCT+6.18
SRFMA0083.3chr1:235097643-235097659TGCCCATATATAGGCT-6.25
Number of super-enhancer constituents: 56             
IDCoordinateTissue/cell
SE_00182chr1:235096120-235101897Adipose_Nuclei
SE_00983chr1:235097261-235098779Adrenal_Gland
SE_01666chr1:235096626-235100084Aorta
SE_02305chr1:235096364-235100538Astrocytes
SE_04136chr1:235096460-235097832Brain_Anterior_Caudate
SE_04136chr1:235097898-235099053Brain_Anterior_Caudate
SE_06052chr1:235096043-235100300Brain_Hippocampus_Middle
SE_07547chr1:235096391-235100017Brain_Hippocampus_Middle_150
SE_08384chr1:235097173-235098864Brain_Inferior_Temporal_Lobe
SE_09160chr1:235089274-235102029CD14
SE_13412chr1:235096493-235101824CD34_Primary_RO01536
SE_14852chr1:235096281-235101639CD4_Memory_Primary_7pool
SE_19577chr1:235096550-235100566CD4p_CD25-_Il17p_PMAstim_Th17
SE_21117chr1:235097106-235100877CD8_Memory_7pool
SE_23314chr1:235096491-235100470Colon_Crypt_1
SE_23955chr1:235097251-235098787Colon_Crypt_2
SE_25800chr1:235089687-235101859Duodenum_Smooth_Muscle
SE_26806chr1:235097145-235100451Esophagus
SE_27663chr1:235089063-235101555Fetal_Intestine
SE_28576chr1:235088850-235101396Fetal_Intestine_Large
SE_29689chr1:235096351-235100491Fetal_Muscle
SE_31235chr1:235096206-235101509Fetal_Thymus
SE_31572chr1:235096504-235100646Gastric
SE_32492chr1:235096171-235101826GM12878
SE_33758chr1:235092170-235101690HCC1954
SE_34767chr1:235092103-235099043HeLa
SE_36952chr1:235097341-235100352HSMMtube
SE_37966chr1:235095673-235098616HUVEC
SE_38924chr1:235096504-235100475IMR90
SE_40307chr1:235097907-235099855K562
SE_40653chr1:235096334-235100704Left_Ventricle
SE_41640chr1:235097171-235098761LNCaP
SE_42265chr1:235096397-235099904Lung
SE_43462chr1:235096235-235101604MCF-7
SE_44202chr1:235096244-235101645NHDF-Ad
SE_44805chr1:235096846-235100768NHLF
SE_45558chr1:235095403-235101783Osteoblasts
SE_47119chr1:235087515-235103374Panc1
SE_47599chr1:235096544-235098759Pancreas
SE_48462chr1:235097280-235101477Psoas_Muscle
SE_48697chr1:235096543-235100576Right_Atrium
SE_50040chr1:235096232-235101854RPMI-8402
SE_50071chr1:235089709-235100691Sigmoid_Colon
SE_51271chr1:235096309-235101796Skeletal_Muscle
SE_51773chr1:235097396-235099619Skeletal_Muscle_Myoblast
SE_52352chr1:235089712-235101497Small_Intestine
SE_53330chr1:235096392-235100521Spleen
SE_54553chr1:235096129-235101782Stomach_Smooth_Muscle
SE_55407chr1:235097231-235099877Thymus
SE_56760chr1:235096269-235098211VACO_400
SE_59259chr1:235089283-235124733Ly3
SE_60969chr1:235059965-235155853HBL1
SE_61435chr1:234961094-235124239Toledo
SE_62329chr1:235047040-235185428Tonsil
SE_63542chr1:235097329-235099682HSMM
SE_65393chr1:235092372-235101616Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1235097868235098070
Number: 1             
IDChromosomeStartEnd
GH01I234953chr1235089124235101946
Enhancer Sequence
TTAAAGAAAA CTTACTTGAG AGTCAGGCAG GAAGGGGAGA TGGGATACAC ACTTTCCCTA 60
TCTTTCAGGT TTCTGCAATC TCAGCGCATG CTGCTTAAGA GGAAAAGAGC AGCAAAGCAG 120
ATGAAAAGCA CTGCATCCTT AAGTGATTTA CCTGTTCCCA AGCAGGCCTG CCTCACACCT 180
GCCTCCCCCC AGTTCCCTGT CATTGACCCT CCCGCCACCA TATCTGTGGC ATCTGGTGTG 240
CTGCACACAC AGTATATGTG TGCAAGTGCA TGGTATATAC ACATAGCACA CATGCATACA 300
TGCTATAAAC ACATGCCCAT ATATAGGCTC AGTGCACAGG TACGCACAGT GCTCAGGTAC 360
ACAGAGTACA CACACCTGCT AGCCACATAC ACTCTCAGTG TACACACATG GTGCTCATGC 420
ACACATGGTA GTGCATGGTG AATCCACATA GCATCCATGC ACACACACAG TACCCACACA 480
CACACGCGGT ACATACACAT GGCACCCCTG CACATACACA GTAGACATGC GTAACCCAGA 540
AAGTGGTTCT TGCTCTCTCT GCAACCTTAA GACTTTGGCA GTTTTTGTTA ACTCCCACAC 600
TTGGCAGGAT TACATTTCCT TGTGGCCTCA ATGACGTGAT AGGGCAGATT TATTGGGCTT 660
ACAGAAAAAA AGAGAGAGGA GAGAGAGCGA GAGAGCGAAC AGTAAACTCT GCTGTGCAGT 720
CAACCTGGAC CTTGGTTTTA AGTTGCACAT CATCAGGGCC AAGAGAGAAG ATTTGGCAAC 780
ATGGGGTGGT TTGGTGAGAG TCGGCATGTT TCACTGGTAA TCTGCTGGAG CACTAAAATA 840
TATACATCCA AAGGTTACCT 860